Mac Bell
2 – 3 minutes
(WHTM) — The U.S. Food & Drug Administration (FDA) has announced the voluntary recall of a sinus nasal wash bottle system following a confirmed test result of microbial contamination.
According to the FDA, Melville, NY. Ascent Consumer Products Inc. is voluntarily recalling one lot of SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System due to a microbial contamination of Staphylococcus aureus (s. aureus).
For those who don’t know, this product is mostly used as a nasal wash of the nasal passages to help temporarily relieve symptoms associated with sinusitis, cold, flu, or allergies.
The FDA says s. aureus contamination can cause various infections for the user, which could be serious and potentially life-threatening.
To date, no adverse events have been reported to Ascent Consumer Products, Inc.
The SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System (lot# 024122661A1) was packaged in a carton, containing the squeeze bottle and 30 Saline Packets. The affected lot was distributed nationwide January 2025 through retail and online outlets.
According to the FDA, distributors and retailers in possession of the affected lot should immediately cease distribution and remove the recalled SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System lot from inventory.
Consumers who have the product should discontinue use and immediately return it to the place of purchase or discard it.
If you have any questions, you can contact Ascent Consumer Products Inc. by email at cs@ascentconsumerproducts.com.
If you have any adverse reactions or quality problems with the use of this product, you can report it to the FDA’s MedWatch Adverse Event Reporting program online or by calling 1-800-332-1088.
CLASS I – HIGH OR MEDIUM RISK
This is a health hazard situation where there is a reasonable probability that the use of the product will cause serious, adverse health consequences or death.
CLASS II – LOW RISK
This is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.
CLASS III – MARGINAL RISK
This is a situation where the use of the product will not cause adverse health consequences or the risk is negligible.
For help with meat, poultry, and egg products, call the toll-free USDA Meat and Poultry Hotline:
007-2025HIGH – CLASS IIMPORT VIOLATION
ACTIVE
TUE, 02/25/2025 – CURRENT
CALIFORNIA, FLORIDA, ILLINOIS, NEBRASKA, NORTH CAROLINA, OHIO, TENNESSEE, TEXAS, WASHINGTON
WASHINGTON, Feb. 25, 2025 – C&T Produce Wholesale Inc., doing business as L&V Food Supply, the importer of record, located in Houston, Texas, is recalling approximately 1,152 pounds of ineligible peppered frozen, dried Siluriformes fish products that were produced by an establishment in Vietnam that is not eligible to export Siluriformes fish to the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. Additionally, the products were not presented for import reinspection into the U.S.
The following product is subject to recall, regardless of the production date [view labels]:
The product does not bear an establishment number nor a USDA mark of inspection. These items were shipped to retail locations in California, Florida, Illinois, Nebraska, North Carolina, Ohio, Tennessee, Texas, and Washington.
The problem was discovered during routine FSIS surveillance activities of imported products at a retail store in California.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Chinh Nguyen, Director, L&V Food Supply at 832-381-0293 or chinhnguyen@ctproduce.us.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.
Raw – Intact
L&V Food Supply
Chinh Nguyen, Director
Soledad Calvino
(202)720-9113
FSISpress@usda.gov
Last Updated: Feb 25, 2025
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“Not just for food, but for high-value products as well, like pharmaceuticals.”
Note: Don’t fool yourself into thinking they’ll label it …EWNZ
The following report was first published on September 17th, 2021, on winepressnews.com.
Scientists are actively creating new foods that are similar to the current Covid vaccines in use, as a way to replace traditional inoculation. Both Pfizer and Moderna Covid vaccines use messenger RNA (mRNA) technology that rewrites a person’s genetic code to fight disease. Moderna refers to this technology as an “app,” “software,” “operating system,” and more.
Currently, mRNA tech used in the Covid vaccines must be stored at cold temperatures to work, or they lose their stability.
However, researchers at the University of California-Riverside are testing ways for this mRNA tech to be functional under normal temperatures. In this case, if they are successful, they would then design plant-based mRNA food for public consumption.
For further development and functionality, the researchers received a $500,000 grant courtesy of the National Science Foundation.
The team seeks to accomplish three goals: first, attempt to successfully carry and transport DNA containing the same mRNA vaccine tech into plant cells, where they can replicate.
From there, the team wants to see if these newly cultured plants can replicate enough to generate sufficient mRNA to replace the traditional injection via syringe. Finally, the group of researchers will establish what the proper dosage will be for the masses to consume to effectively replace vaccinations.
Juan Pablo Giraldo, an associate professor in UCR’s Department of Botany and Plant Sciences, said in a university release:
“Ideally, a single plant would produce enough mRNA to vaccinate a single person.
“We are testing this approach with spinach and lettuce and have long-term goals of people growing it in their own gardens. Farmers could also eventually grow entire fields of it.”
In order for this to work properly, the plant’s chloroplasts are key, says Giraldo and a team of scientists from UC-San Diego and Carnegie Mellon University. Chloroplasts are tiny organs inside plant cells that aid in the conversion of sunlight into usable energy.
“They’re tiny, solar-powered factories that produce sugar and other molecules which allow the plant to grow. They’re also an untapped source for making desirable molecules,” Giraldo added.
Previous studies have been reported to have shown gene expression, which is not a natural part of the plant. This was discovered when Giraldo and his team successfully injected genetic material into the chloroplasts.
Professor Nicole Steinmetz of UC-San Diego worked with Giraldo and the team to utilize nanotechnology to help deliver even more genetic material – identical to how the Covid vaccines work, not just the Moderna or Pfizer ones either.
“Our idea is to repurpose naturally occurring nanoparticles, namely plant viruses, for gene delivery to plants. Some engineering goes into this to make the nanoparticles go to the chloroplasts and also to render them non-infectious toward the plants,” Steinmetz explained.
Giraldo added:
“One of the reasons I started working in nanotechnology was so I could apply it to plants and create new technology solutions. Not just for food, but for high-value products as well, like pharmaceuticals.”
In light of these new ambitions to put mRNA technology into food, it gives a whole new perspective to the saying, “You are what you eat:” If you eat GMOs, you are a GMO.
As far as I am aware of, I have not heard much on this line of development, but that is not to say mRNA foods won’t become more mainstream and commercialized at some point. Whatever the case, don’t consume them, don’t get injected with this technology.
Proverbs 4:14 Enter not into the path of the wicked, and go not in the way of evil men. [15] Avoid it, pass not by it, turn from it, and pass away.
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Do not sell or serve Lyons ReadyCare and Sysco Imperial Frozen Supplemental Shakes. FDA’s investigation is ongoing.
All frozen supplemental shakes under brands Lyons ReadyCare and Sysco Imperial within shelf-life.
Frozen supplemental shakes under brands Lyons ReadyCare and Sysco Imperial were sold to institutional settings such as long-term care facilities (LTCF).
Symptoms usually start within two weeks after eating food contaminated with Listeria but may start as early as the same day or as late as 10 weeks after. Mild symptoms may include a fever, muscle aches, nausea, tiredness, vomiting, and diarrhea. If the more severe form of listeriosis develops, symptoms may include headache, stiff neck, confusion, loss of balance, and convulsions.
Frozen supplemental shakes were distributed to foodservice customers, including hospitals and long-term care facilities.
Ongoing.
February 21, 2025
The FDA and CDC, in collaboration with state and local partners, are investigating illnesses in a multistate outbreak of Listeria monocytogenes infections linked to Lyons ReadyCare and Sysco Imperial Frozen Supplemental Shakes.
On November 25, 2024, FDA was notified about an outbreak of Listeria monocytogenes in the United States, with many ill people residing in long-term care facilities (LTCF) prior to illness onset. FDA’s traceback investigation identified that each of the LTCF who supplied invoice information for review from 2024 to present received a frozen supplemental shake of either Lyons ReadyCare or Sysco Imperial brand. As part of this investigation, FDA collected environmental samples and found the outbreak strain of Listeria.
According to CDC, this outbreak includes cases dating back to 2018, with 20 cases across 2024 and 2025, and is currently ongoing. Epidemiologic evidence in previous investigations were unable to identify a source of the outbreak. As of February 21, 2025, a total of 38 people infected with the outbreak strain of Listeria monocytogenes have been reported from 21 states. Of the 38 people for whom information is available, 37 people have been hospitalized. Eleven deaths have been reported. Of the 38 people for whom information is available, 34 (89%) reported living in long term care facilities or were hospitalized prior to becoming sick. Records reviewed from facilities indicated nutritional shakes were available to residents.
FDA has been informed that certain Lyons ReadyCare and Sysco Imperial Frozen Supplemental Shakes are being voluntarily recalled. FDA is working with the recalling firms. FDA’s investigation is ongoing, and more information will be provided as it becomes available.
Total Illnesses: 38
Hospitalizations: 37
Deaths: 11
Last Specimen Collection Date: January 23, 2025
States with Cases: AL, CA, CO, CT, FL, IL, IN, MD, MI, MN, MO, NC, NV, NY, OH, OK, PA, TN, TX, WA, and WV
COMPANY ANNOUNCEMENT
When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company’s announcement as a public service. FDA does not endorse either the product or the company.
Company Announcement Date: February 18, 2025 FDA Publish Date: February 20, 2025 Product Type: Food & Beverages
Allergens Reason for Announcement:
Recall Reason Description
Undeclared allergen (wheat, eggs, milk) Company Name: ZB Importing LLC Brand Name: Product Description:
Product Description
Snack rolls, biscuits, and wafers
ZB Importing LLC is voluntarily recalling certain lots of six varieties of Ulker Brand snack rolls, biscuits, and wafers due to undeclared wheat, egg and/or milk in the Ingredient List and/or Contains Statement on the product labels. People who have an allergy or severe sensitivity to wheat, egg, or milk run the risk of a serious or life-threatening allergic reaction if they consume these products.
Products were distributed through retail stores in Ontario, Canada and the following US states AL, AR, CA, CT, CO, DC, DE, FL, GA, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, NE, NC, NH, NJ, NM, NY, OH, OK, PA, RI, SC, TN, TX, VA, WA, WI and WV.
This mislabeling was discovered following receipt of a single consumer complaint involving an allergic reaction. The issue originated from a supplier who inadvertently failed to fully disclose all allergens while translating the ingredient list. We are actively working with the supplier to implement stricter labeling controls, including an additional verification process for multilingual labels.
Consumers who have purchased any of the below Ulker Brand products are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at info@ziyad.com.
See Product List
U.S. — As an added safety measure to prevent further runway catastrophes, Delta Airlines has added a little hanging tennis ball to the end of runways to help female pilots.
After multiple recent incidents of female pilots struggling to figure out exactly when a runway begins and ends, Delta decided to begin positioning cranes to hang tennis balls from a string at the end of each runway.
“A tennis ball on a string is the most trusted technique in the world to keep women from wrecking,” explained Delta CEO Ed Bastian. “Millions of women have been stopped from smashing their cars into the garage wall by husbands graciously hanging up a tennis ball. We are excited to bring this tried-and-true technology to Delta Airlines to hopefully keep our female pilots from wrecking any more planes.”
According to airport personnel, the tennis ball on a string has already prevented over a dozen crashes by female pilots. “Now, if we can just get those lady pilots to stop checking their makeup and focus on the instrument panel,” said air traffic controller Bob Rendon. “Hang on a minute, got a girl pilot coming in hot — stop when you touch the tennis ball, I repeat, brake for the tennis ball!”
At publishing time, a female pilot in Toronto had called her husband to say she might have gotten a slight scratch on her plane.
www-silive-com.cdn.ampproject.org
By Mike Matteo | mmatteo@siadvance.com
STATEN ISLAND, N.Y. — Toyota has issued a safety recall for vehicles under its own badge and under its luxury vehicle brand, Lexus.
The company is currently recalling certain model years of its Camry sedan, along with a number of RX and NX SUVs from Toyota’s high-end Lexus line, over seat belt issues, with over 40,000 potentially affected vehicles, according to the National Highway Traffic Safety Administration (NHTSA).
The 40,922 vehicles that are affected were sold under model years 2024 and 2025. The recall covers the following cars: 2024-2025 Lexus RX and RX hybrid, 2025 Lexus NX and NX hybrid and 2025 Toyota Camry, according to the recall notice.
The recall is due to the seat belts in the second row center seat, which might have been damaged before being installed.
The damaged seat belts could fail during a crash and increase the risk of a serious injury.
Toyota is advising that owners of affected vehicles can bring them to a dealership, where the dealer will inspect the seat belts and replace them if necessary.
The company will fully notify affected owners of the recall beginning mid-March, according to the notice.
Owners can contact Toyota customer service at 1-800-331-4331, or or the NHTSA vehicle safety hotline at 1-888-327-4236 to see if their car is affected by the recall.
Recently, Toyota had to issue recalls for some of its most popular models, including the Tacoma pickup and Sienna minivan.
Certain model years are believed to have issues with the rear brakes, which could lead to a fluid leak, hinder brake performance and increase the risk of a crash, according to documents filed with the the NHTSA.
The Sienna minivan recall is due to issues with bolts connecting rear seats, according to a press release from Toyota.
Toyota Siennas with model years between 2021 and 2025 fall under the recall.
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Ivanhoe Newswire
ORLANDO, Fla. (Ivanhoe Newswire) — February is American Heart Month. And what better time to talk about heart health?
Did you know heart disease claims a life in the U.S. every 37 seconds? Research from the American Heart Association has found that nearly half of all adults in the U.S. have some form of cardiovascular disease. While you may already know the main culprits behind heart disease like high blood pressure, high cholesterol, obesity, and a history of smoking, there are other unexpected risk factors that can have a big impact on your heart health.
“I’m going up the stairs and I’m pulling myself up the stairs,” recalled Vickey Soennichsen.
She was having a heart attack.
It happens to more than 800,000 people each year. But one in five heart attacks is silent and the person isn’t aware of the damage that’s being done.
“I had a patient who had a toothache that turned out to be her symptom for having a heart attack,” said Annabelle Santos Volgman, MD, cardiologist at Rush University Medical Center.
That’s not the only thing you need to know, where you live plays a crucial role. The American Heart Association found southern states have the highest rate of death by heart disease. They believe it’s because more people live in poverty, with less access to fresh fruit, safe places to walk, or access to healthcare.
The quality of your tap water also has an impact. Researchers at Columbia found people exposed to high levels of arsenic in their drinking water were 42% more likely to develop heart disease.
But don’t replace water with diet soda. Women over 50 who drink two or more diet sodas or any kind of artificially sweetened drinks a day face an increased risk of stroke and heart attack.
Even what happens during pregnancy impacts a woman’s heart health. Complications like gestational hypertension, pre-eclampsia, preterm birth, and gestational diabetes significantly increase the risk of developing cardiovascular disease later in life. And if a woman hits menopause before they turn 42, new research shows the odds of having a heart attack or stroke may be twice as high than if you go through it later.
Meanwhile, having constant low-level stress can cause you to be 40% more likely to have a heart attack. The doctor’s best advice? Surround yourself with good people and be good to yourself.
If you think heart disease begins in our 50s, think again. A study published in JAMA found that heart health begins to decline around age 10 if children have unhealthy lifestyles. This includes poor diet, lack of exercise, and smoking. These early habits significantly increase their risk of heart attacks and strokes later in life.
Contributors to this news report include: Marsha Lewis, Producer; Roque Correa, Editor.
A racist, former Survivor contestant and tobacco progressive sued the president claiming that unless we castrate the kids, they’ll die. And a judge ruled in front of a courtroom full of transgender activists cheering for child mutilation that banning castration wasn’t constitutional.
Where is child castration mentioned in the Constitution?
The closest that the matter came to the attention of the Founding Fathers was when Thomas Jefferson authored a Virginia state bill punishing rape with castration. What Jefferson thought fitting for rapists, modern day members of his party believe is fitting for young children.
The progressive child castration complex may be on the wrong side of history, sanity and decency, but so long as it has enough lawyers and judges, it will go on wielding the scalpel.
Trump’s “Protecting Children from Chemical and Surgical Mutilation” executive order had temporarily ended the practice, opposed now even by most Democrats, of performing experimental, deadly and destructive transgender procedures on minors.
In the latest New York Times poll, 71% of Americans and even 54% of Democrats opposed castrating kids in the name of transgender ideology. Only 10% of Americans and only 19% of Democrats supported the extreme leftist position adopted by most Democrat politicians of performing these experimental procedures on children as young as 10 years old. (In actual practice, transgender tracking is being practiced even on toddlers.)
However Attorney General Keith Ellison of Minnesota, a former devout member of the racist Nation of Islam, who had been accused of abuse by two women, Attorney General Nick Brown of Washington, a former Survivor contestant and Biden nominee, and Attorney General Dan Rayfield of Oregon, funded by tobacco money, didn’t get the memo and sued the Trump administration for the right to go on castrating kids.
“If the Order stands, transgender children will die,” the three attorneys general complained.
The ‘order’ being an executive order that banned castrating ‘children’ for their ideological pleasure. No child dies because he or she isn’t subjected to unnecessary surgery promoted by adults for political reasons that will leave him or her unable to have children or live a normal life.
The only thing that will ‘die’ from a castration ban is the lucrative income derived by some hospitals and doctors from performing these horrifying experiments on children, and what will also die is a major ideological plank of identity politics that insists sex is entirely subjective.
And women don’t really exist.
The British government already disproved the lie that a ban on experimental castration drugs (often misleadingly described as ‘puberty blockers’) leads to a rise in suicide rates. After lies spread by transgender identity activists, a review of the data in the UK showed no such rise.
The Trump executive order follows in the footsteps of similar moves in the UK and Europe.
Despite that three AGs for castrating kids argued that, “whatever interest the federal government may have in cutting off treatment to transgender kids during the pendency of this case pales in comparison to Plaintiffs’ irreparable harm.”
The interest of the federal government is in preventing irreparable harm to kids. Delaying castration meds or other destructive procedures does not cause harm to children. Acting on them does. The only irreparable harm in transgender procedures is in their implementation.
Despite that, Judge Lauren King, a Biden nominee, claimed that preventing hospitals from castrating kids for profit won’t survive “constitutional scrutiny” to the applause of a courtroom packed with transgender activists cheering for child mutilation.
Certainly if there’s anything that James Madison and the Framers had in mind for the Constitution was that it must absolutely protect child castration. And while those words may not appear in the text, surely they’re there in a penumbra, right next to a right to kill unborn children.
According to the three attorneys general and Judge Lauren, banning the castration of children, counts as discrimination on account of sex. This is a little confusing because those same people also claim that sex doesn’t exist. Or at least it exists only in its absence. If women don’t exist, they can’t be sexually discriminated against. However transgenders do exist and thus the entire body of sexual discrimination civil rights was really meant to protect transvestites.
Certainly if there’s anything the feminist leaders of the 1960s were after, it was protecting the rights of men to go into women’s locker rooms and drive them out of professional sports.
The stupid civil rights trick employed by Judge Lauren and transgender activists is to argue that a ban on everything from castrating kids to stopping male sex offenders from raping women in prison is discrimination on account of sex. And the only way to undo discrimination on account of sex is to let male boxers beat up women and Munchausen-by-proxy mothers turn their little boys into little girls. Anything else is a civil rights violation.
But if stopping assaults on women and children is a civil rights violation, then civil rights has been inverted into a horrid monstrosity that oppresses the weak and the vulnerable.
That seems to be the only option that Democrats are giving their own voters and supporters.
Judge Lauren complained that Trump’s “Protecting Children from Chemical and Surgical Mutilation” aims at the “erasure of trans individuals”. This isn’t judicial language, it’s activist rhetoric. The lawsuit and the ruling weren’t following the law, but following identity politics.
The truth is that identity politics invented a new victim class that it is sustaining with the suffering and mutilation of children and the abuse of women. That’s why even most Democrats have turned against the transgender movement. It’s one reason some of them voted for Trump.
There is no “erasure of trans individuals”. If a group has to be manufactured by imagination and medical intervention, whose only scientific basis is heated rhetoric, it doesn’t actually exist. It’s the transgender movement that is actually dedicated to taking healthy and functioning people and using them to erase sex differences and 99% of the population of men and women.
That’s why pronouns have been inflicted on 99.99% of society, why slurs like “cishet” have been formalized to make the normal seem abnormal, and why transgender ideology continues to be inflicted in the most destructive ways on the most vulnerable members of our society.
Rather than conducting a reckoning with the damage, instead of thinking of the children they have harmed, they cry to the courts, “won’t someone think of the castrating the children”.
And the courts answer, “sharpen your scalpels”.
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Danielle DeAngelis
2 minutes
Check your freezer ASAP.
Published on February 19, 2025 Photo:
Getty Images. EatingWell design.
Trader Joe’s just announced a recall on a popular frozen breakfast item, according to a recent company announcement.1 This is due to a potential foreign matter contamination.
The product affected is the brand’s 10-ounce Organic Acai Bowls with berries, bananas, granola and dried coconut. All units of this product are impacted by this recall. The smoothie bowls are being recalled because they may contain pieces of plastic, causing a choking or injury hazard.
Consumers with this product should dispose of it or return to their local Trader Joe’s for a refund. If you are experiencing any injury or illness after eating this recalled frozen food, contact your health care provider.
For questions about this recall, call Trader Joe’s Customer Relations at (626) 599-3817 or fill out the grocery chain’s product feedback form online.
EatingWell uses only high-quality sources, including peer-reviewed studies, to support the facts within our articles. Read our editorial process to learn more about how we fact-check and keep our content accurate, reliable and trustworthy.
February 15, 2025 – Wild Coast Raw Pet Food has been identified as the source of a bird flu infection in house cats in Oregon.
The cats became ill in early February after consuming raw pet food manufactured by Wild Coast LLC. Sadly, their illness was so severe they had to be euthanized.
The Oregon Department of Agriculture collected samples from the affected cats pre- and post-mortem, and from open containers of the raw pet food. Tests confirmed the presence of Highly Pathogenic Avian Influenza (HPAI or bird flu) in both cats and the food samples.
The Washington State Department of Agriculture issued a public health alert warning on Friday specifically about Wild Coast Raw Boneless Free Range Chicken Formula with lot numbers 22660 and 22664 and the best by date December 2025.
Pets with bird flu infections may have a fever, lethargy, low appetite, reddened or inflamed eyes, discharge from the eyes and nose, difficulty breathing, and/or neurological signs like tremors, seizure, incoordination, or blindness.
The WSDA recommends cat parents contact their veterinarian immediately if their cat has consumed the affected Wild Coast Raw product.
Officials have not linked the handling of raw pet food products to human bird flu infections. However, people can become infected if the virus enters through their eyes, nose or mouth.
Current human health risks are low, but the alert says people exposed to bird flu should monitor themselves for symptoms such as eye redness or irritation, cough, sore throat, sneezing, runny/stuffy nose, muscle/body aches, headaches, fatigue, fever, trouble breathing, diarrhea, nausea and/or vomiting.
Although the FDA has not released a statement about this issue yet, it does encourage consumers to report complaints about pet food products. You can do this electronically through the Safety Reporting Portal or visit the SmartHub – Safety Intake Portal – Report a Product Problem (fda.gov) to obtain electronic assistance.
Canadians can report any health or safety incidents related to the use of this product by filling out the Consumer Product Incident Report Form.
U.S. citizens can report complaints about FDA-regulated pet food products by calling the consumer complaint coordinator in your area.
Or go to the FDA’s “Report a Pet Food Complaint” page.
Canadians can report any health or safety incidents related to the use of this product by filling out the Consumer Product Incident Report Form.
Get free cat food recall alerts sent to you by email. Subscribe to the Cat Food Advisor’s emergency recall warning system.
Cancel any time.
Product:
Wild Coast Raw Boneless Free Range Chicken Formula
Date of warning:
February 15, 2025
Manufacturer:
Wild Coast LLC
Reason:
Bird Flu Contamination
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"OUR WORLD" 
