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FDA’s Food Safety Modernization Act (FSMA) Rule 204 approaching, restaurant operators stand to gain improved confidence in the safety and quality of the food they serve. Steps to Strengthen Positioning To prepare for FSMA Rule 204, begin by identifying the foods you purchase that are on the FDA’s Food Traceability List.
Food and Drug Administration (FDA) has issued two temporary food labeling guidance documents that attempt to balance industry supply and demand during the novel coronavirus pandemic. The requirements apply to products, including ingredients, that are typically purchased by restaurants to further prepare for sale to consumers.
The FDA issued this warning this morning – Recall underway. The FDA has reviewed and supports NCDHHS’s analytical findings and found that analytical results at this level could result in acute toxicity. Product WanaBana apple cinnamon fruit puree pouches, all lot codes and expiration dates.
Food & Drug Administration (FDA) has updated and released a best practice guide focused on food and beverage service during the COVID-19 pandemic. Other emergency orders have relaxed restrictions on purchases of alcohol inventory on credit or consignment, which may prove crucial to smaller restaurants.
The FDA says the strawberries were branded FreshKampo and HEB, but again give no indication where the strawberries were grown. People who purchased FreshKampo and HEB fresh organic strawberries between March 5, 2022, and April 25, 2022, and then froze those strawberries for later consumption should not eat them. Canadian Co-op.
September 28, 2023 The Canadian Food Inspection Agency (CFIA) is advising businesses to avoid selling and purchasing tara protein powder (tara flour), or products containing this ingredient. This just landed in my inbox.
The scallops were purchased by restaurants, distributors, and food retailers in Illinois, Massachusetts, New Jersey, New York, and Pennsylvania and may have been further distributed. According to the FDA, Intershell International Corp. 4, 2024, but may still be on hand at purchasers’ locations. 26, 2023, Dec. 27, 2023, and Jan.
Report your illness to the FDA. Here are the links: Phone the FDA Main Emergency Number at 866-300-4374 or phone the Consumer Complaint Coordinator for your state or area. DO NOT, as Daily Harvest suggested, “to dispose of it.” The product can be tested for pathogens, allergens and chemicals. Do not eat the product.
The FDA is alerting parents and caregivers about two varieties of LittleOak infant formulas that the company is currently recalling. Parents and caregivers of infants who have purchased these products should understand that they have not been evaluated to determine whether they meet U.S. food safety and nutritional standards.
With the increased number of hand sanitizing brands entering the market, it is extremely important to ask the right questions to ensure the quality of the product you are purchasing and to have confidence that it will be available for years to come. What lab testing has been done to date? And what is the shelf life?
Under the Court’s ruling, foie gras could be legally sold to California consumers provided that the seller is located outside of California, the foie gras being purchased is not present within California at the time of sale, the transaction is processed outside of California, and payment is received and processed outside of California.
The Food and Drug Administration (FDA) has issued a warning about certain tejocote root supplements substituted with toxic yellow oleander. Tested Products: To date, the FDA has tested 9 samples, representing the 9 different products listed below, and found them to contain yellow oleander. Additional sample analysis is pending.
According to the details posted online by the FDA, the recall was initiated on June 16, 2023, and is ongoing. Recalled products: Romaine lettuce packed in bulk 45-pound mini-bins 2580 mini-bins Code: Tierrasol 23-26R08 Anyone who purchased the recalled product should immediately dispose of it and not consume it.
Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for various soup and bowl products that may be contaminated with foreign material, specifically wood, in an FDA-regulated ingredient, cilantro. These products should be thrown away or returned to the place of purchase.
FDA is aware that, as of December 13, recalled WanaBana Apple Cinnamon Puree product (including recalled three packs) was still on the shelves at several Dollar Tree stores in multiple states. This product should not be available for sale and consumers should not purchase this product.
The recall is the result of a routine sampling program by the FDA. Consumers who have purchased “Swad Cinnamon Powder 3.5OZ” are urged to return it to the place of purchase for a full refund. The FDA issued warnings on March 6 about the Swad cinnamon and several other brands, some of which are being recalled.
NBC News viewed an email it sent Friday asking a customer to throw away the lentils “out of an abundance of caution” and offering a $10 credit for every bag of the product that was purchased. . “A and the FDA has initiated an investigation. Starting in late 2021 Lucky Charms food poisoning reports started to trend on iwaspoisoned.com.
Consumers who have purchased El Chilar Ground Cinnamon “Canela Molida” with lot code D300 EX1024 and F272 EX1026 are urged to stop using the product immediately and to return it to the place of purchase for a full refund.
Business owners have 15 days to respond to FDA warning letters. The FDA inspected your manufacturing facility, located at 10849 Midwest Industrial Blvd. The FDA inspected your manufacturing facility, located at 10849 Midwest Industrial Blvd. Louis, MO In a Nov. 9 warning letter to Wan-Gee Foods Inc.
Jones is scheduled to begin at the FDA on September 24, 2023. He also led several national sustainability programs, including the EPA’s Environmental Preferable Purchasing Program and the Presidential Green Chemistry Awards Challenge. I’m delighted to welcome Jim to the FDA. Califf, M.D.
FDA Recalls [link] HH Fresh Trading Corp Recalls Taiwan Enoki 200gx25pk Because of Possible Health Risk Summary Company Announcement Date: November 01, 2024 FDA Publish Date: November 02, 2024 Product Type: Food & Beverages Reason for Announcement: Potential to be contaminated with Listeria monocytogenes.
Recalls Chicken Salad on White Sandwich Due to Undeclared Milk Allergen Summary Company Announcement Date: March 27, 2025 FDA Publish Date: March 27, 2025 Product Type: Food & Beverages Reason for Announcement: Undeclared milk Company Name: Cromer Food Services, Inc. Cromer Food Services, Inc., link] Cromer Food Services, Inc.
The FDA is cautioning pet owners not to feed their pet’s certain Aunt Jeni’s Home Made frozen raw pet food “as it poses a serious threat to consumer and animal health” because of Salmonella Infantis contamination. If consumers have the product and cannot determine the lot code, the FDA recommends that the product be thrown away.
FDA is conducting an onsite inspection at the Austrofoods facility located in Ecuador. FDA will update this advisory to share the sample results once the analysis is complete. Working together with Ecuadorian authorities, the FDA has confirmed that, of Negasmart’s direct customers, only Austrofoods ships product to the US.
of Middleburg, FL, is recalling its Nuez de la India Seeds because FDA analysis has determined that the seeds appear to be Thevetia peruviana, or yellow oleander. The recall was the result of sampling conducted by the FDA. Consumers who purchased Nuez de la India seeds from Todorganic Inc. Todorganic Inc. 12 seeds in a bag.
Food & Drug Administration (FDA) and the U.S. March 17, 2025 Nestl USA is initiating a voluntary recall of a limited quantity of Lean Cuisine and STOUFFERS frozen meals due to the potential presence of wood-like material. For any further support needed, please contact Nestl USA at (800) 681-1676 Monday-Friday from 9 a.m.-6
Based upon the products containing the ingredient konjac powder and the dimensions, FDA has determined that the products present a choking hazard. Consumers who have purchased these products should return them to the store of purchase for a refund. (To The recalled jelly bars were distributed to retailers nationwide.
The firm is working with the FDA. These products are no longer in commerce and are past their sell by date, but consumers should check their freezers and dispose of product or return to store where they purchased for refund. The firm is working with the FDA. link] Gracie’s Kitchen’s Inc. No illnesses have been reported to date.
EPA’s James “Jim” Jones was named Wednesday as the first FDA Deputy Commissioner for Human Foods. FDA Commissioner Robert Califf, who came on board in February 2022, had little choice but to work on a reorganization plan. Jones is scheduled to begin at the FDA on Sept. I’m delighted to welcome Jim to the FDA.
Business owners have 15 days to respond to FDA warning letters. Cooperstown Cheese Company LLC Milford, NY A food firm in New York is on notice from the FDA for serious violations of the Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Human Food regulation.
The CDC and FDA have different data sources, so the counts reported by each agency will not directly correspond. In addition, some people affected by the contaminated product might be reflected in both the numbers reported by the FDA and the numbers reported by the CDC, so the numbers should not be added together.
and the FDA has initiated an investigation. The FDA approached the issue a bit more obliquely, noting that there has not been found a pathogen or cause of the illness (now numbering 446 ‘adverse event reports’) linked to “Dry Cereal.”. Now there are reports of over 6,400 sick. Patrick’s Day. ”.
Discussions with the US Food and Drug Administration (“FDA”) confirmed this. Discussions with the US Food and Drug Administration (“FDA”) confirmed this. Recalled products should be thrown out or destroyed so they may not be consumed or returned to the point of purchase.
FDA is aware that, as of December 7, recalled WanaBana Apple Cinnamon Puree product (including recalled three packs) was still on the shelves at several Dollar Tree stores in multiple states. This product should not be available for sale and consumers should not purchase this product.
Through a private lab, we have been testing dozens of French Lentil + Leek Crumbles and Pineapple and Mango Smoothie samples – as has the FDA and presumably Daily Harvest and Revive. The first lawsuit filed by a Tulsa woman that purchased the Daily Harvest product on May 3 and consumed it on May 7. The hunt continues.
According to the details published online by the FDA, the recall was initiated on July 20, 2023, and is ongoing. Regal Foods, Inc of Leola, PA, is recalling various seasonings because rodent feces were found in samples of oregano. The recalled products were distributed in Georgia, Maryland, Pennsylvania and Kentucky.
The recall was initiated after an FDA inspection. The recall was initiated after an FDA inspection. Production of the product has been suspended until the FDA and Monkey Spit are certain that the problem has been corrected. Swamp Mob BBQ Sauce - because it may contain undeclared soy.
According to the details posted online by the FDA, the recall was initiated on June 16, 2023, and is ongoing. PBM Nutritionals, LLC is recalling Parent’s Choice brand Sensitivity Premium Infant Formula and Tippy Toes brand Sensitivity Premium Infant Formula because of an inadvertent release of rejected product to the market.
Consumers would have been able to purchase these chips as early as November 3, 2024. Frito-Lay has informed the FDA of this action. bags of Lays Classic Potato Chips that may contain undeclared milk, after being alerted through a consumer contact. No allergic reactions related to this matter have been reported to date.
The FDA, along with CDC and state and local partners, are investigating a multistate outbreak of Salmonella Senftenberg infections linked to certain Jif peanut butter products produced at the J.M. FDA conducted Whole Genome Sequencing (WGS) analysis on an environmental sample collected at the Lexington, KY, J.M.
CIBUS Fresh has informed the FDA of this recall and is working with customers to ensure the impacted product is removed from store shelves and is no longer distributed. If consumers believe they have purchased a recalled item, they should dispose of the product and not consume it or return it to the place of purchase for a full refund.
Guenther & Son LLC Issues Allergy Alert on Undeclared Egg in 365 Whole Foods Market Small Bites Macaroni & Cheese Summary Company Announcement Date: March 14, 2025 FDA Publish Date: March 14, 2025 Product Type: Food & Beverages Reason for Announcement: Undeclared eggs Company Name: C.H. [link] C.H.
Consumers who have purchased these products should not consume the products and are urged to return them to the place of purchase for a full refund or discard the product. Smoked salmon has a history of Listeria monocytogenes contamination, especially when it is sliced.
FDA issued a Warning Letter to Wan-Gee Foods of St. Food and Drug Administration (FDA) inspected your manufacturing facility, located at 10849 Midwest Industrial Blvd. At the conclusion of the inspection, the FDA investigators issued an FDA Form 483 (FDA-483), Inspectional Observations.
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