Costco’s Kirkland Signature Women 50+ multivitamins were recalled in Canada for possible metal pieces.
Nephronex liquid multivitamins were recalled in 24 U.S. states and regions due to contamination.
Moringa capsules were linked to a Salmonella outbreak, causing 18 illnesses and seven hospitalizations.
Massachusetts-based company Kettle Cuisine announced the recall this week for the 24-oz cups of Whole Foods Market Kitchen Minestrone Soup. The soup may contain shrimp, which was not listed on the label. Anyone with a shrimp or crustacean allergy could suffer a life-threatening allergic reaction, according to the announcement from the U.S. Food and Drug Administration (FDA).
Company Announcement Date: May 22, 2026 FDA Publish Date: May 23, 2026 Product Type: Food & Beverages
Foodborne Illness Reason for Announcement:
Due to contamination of Salmonella Company Name: SKS Copack Brand Name:
Angel Specialty Products, Royal Gold, Boba Time, Fanale, Denda Product Description:
Specialty Beverages
More milk powder related recalls – What started as an April 20 California Dairies Inc. recall of more than 2 million pounds of dry milk and buttermilk powder—due to potential Salmonella contamination—has since triggered a multitude of seasoning recalls involving products that used the powder as an ingredient.
Most of the affected products were pulled from shelves between late April and mid-May, including one sold at Walmart. As of May 21, the U.S. Food and Drug Administration (FDA) has classified the following recalls as Class I incidents:
- Blackstone Parmesan Ranch Seasoning
- Williams Sonoma Popcorn Sampler Gift Box, containing a White Cheddar Seasoning component
- Wildlife Sour Cream & Onion seasoning
- Pork King Good Sour Cream & Onion Seasoning
FOR IMMEDIATE RELEASE Mogo Moringa LLC Announces Voluntary Recall of Select Lots of Moringa Capsules Due to Possible Salmonella Contamination.
Saint Louis, MO — May 25, 2026 — Mogo Moringa LLC, based in Saint Louis, Missouri, is voluntarily recalling specific lots of its Mogo Moringa Capsules after discussions with the U.S. Food and Drug Administration (FDA) regarding a possible Salmonella contamination concern. This voluntary action reflects the company’s commitment to transparency, cooperation, and maintaining high product quality standards.
The product is packaged in a white plastic bottle and sold online through authorized channels. Mogo Moringa LLC does not authorize any third‑party sellers to distribute its products, and customers are encouraged to purchase only from official sources.
Independent third‑party laboratory testing was conducted on retained samples from the affected lots, and no Salmonella was detected. The company is proceeding with this voluntary recall as a precaution and in coordination with the FDA while the agency continues its evaluation.
The recall applies only to the specific lots listed below:
Affected Lots: • Lot 15525AA – Exp 06/2027 • Lot 00926AA – Exp 01/2028
No other lots or Mogo Moringa LLC products are included in this recall.
Consumers who have product from the affected lots are recommended not to use the product.
Total Nutrition Inc. of Deer Park, NY is voluntarily recalling TNVitamins Ultra Potent Complete Green Superfood and Doctor’s Pride Complete Green Superfood Ultra Potent Moringa Capsules (120 count) because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
The recalled product was distributed nationally through the online platforms, Amazon, Walmart, TikTok Shop, Target, and the company’s websites, http://www.tnvitamins.com/, and https://www.doctorspride.com/.
JXK Enterprises, Inc Issues Voluntary Nationwide Recall of Boner Bears Chocolate Due to Undeclared Sildenafil
JXK Enterprises, Inc is voluntarily recalling Boner Bears Chocolate, Lot #BB21125, after being notified that FDA laboratory analysis confirmed the presence of sildenafil, an active ingredient in the FDA-approved prescription drug Viagra, which is not declared on the product label.
Raaw Energy Expands Recall of Dog Food Because of Listeria Monocytogenes Health Risk
Raaw Energy is voluntarily notifying the public of a recall involving products produced between 7/17/25 and 12/23/25 due to possible Listeria contamination. Another batch date is 3.31.26 Beef and Turkey Medley. While not all products from this period tested positive, this action is being taken out of an abundance of caution. Some products produced during this timeframe were not tested, and bacterial presence was identified during the same period. As a result, products manufactured within these dates could possibly be affected.
Consumers are advised not to use, sell, or consume any affected product. Please discard these items immediately to help reduce the risk of illness.
Dog food distributed nationwide recalled over plastic contamination worries: FDA NewsNation The Food and Drug Administration (FDA) announced that Allprovide Pet … The FDA said the company distributed the dog food nationwide. More …
Dexcom Uncovers Theft of Scrapped Product, Notifies Potentially Impacted Users
Through ongoing quality and accounting reviews, Dexcom discovered two lots of scrapped product were stolen by a third party before destruction and sold into the market.
Insulet Initiates Voluntary Medical Device Correction for Certain Omnipod® Pods in the U.S. and Affected International Markets
ACTON, Mass.–(BUSINESS WIRE)– Insulet Corporation, Inc. (NASDAQ: PODD) (“Insulet” or the “Company”) today announced a voluntary Medical Device Correction for specific lots of Omnipod® 5, Omnipod DASH®, and Omnipod® Insulin Management System (Omnipod Eros) Pods due to a manufacturing issue, identified through ongoing product monitoring, that could result in insulin under-delivery.
FDA confirms Class I recall for vascular device used by cardiologists and surgeons
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| Product Description | Recall Class | FDA Recall Posting Date | Recalling Firm |
|---|---|---|---|
| Z-2227-2026 – Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12 (722067), Azurion 7 B20 (722068), Azurion 7 M12 (722078), Azurion 7 M20 (722079, … | 2 | 05/21/2026 | FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-2229-2026 – Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-Nicol (722030), Integris Allura 15 & 12 (monoplane) (722043), INTEGRIS Allura 15-12 (biplane) (722044… | 2 | 05/21/2026 | FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-2228-2026 – Allura system; System Code Description (Model Numbers): Allura Xper FD10C (722001), Allura Xper FD10F (722002), Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10/10 (722005, 722011, 722027),… | 2 | 05/21/2026 | FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
Better Weather Actives LLC Recalls Better Weather Fix Elixir Due to Undeclared Mitragynine and Mitragynine Pseudoindoxyl
FOR IMMEDIATE RELEASE – May 28, 2026 – Sheridan, Wyoming. Better Weather Actives LLC is voluntarily recalling ALL lots of Better Weather Fix Elixir 15 ml because the products may contain undeclared Mitragynine and Mitragynine Pseudoindoxyl (MP). MP is a more potent derivative of Mitragynine, or Kratom. Consumption of MP can produce undesirable effects such as nausea, vomiting, rapid heart rate (tachycardia), palpitations, hallucinations, sedation, anxiety, and loss of consciousness. It can also fatally suppress the respiratory system. Consumption of Mitragynine, especially MP, may cause addiction with severe opioid withdrawal symptoms. Consumption of products that contain Mitragynine or MP, especially in the context of concomitant use of other drugs (prescribed or illicit), could result in other severe or fatal physiological effects.
The company has not received any reports of adverse events related to this recall to date. The recalled products are packaged in 15 ml bottles packed in display boxes labeled “Better Weather Fix Elixir” and “Better Weather Fix Elixir Berry.”. The recalled products were sold at the consumer level nationwide.
Over 285,000 packages of Gas-X Simethicone 125 mg SoftGels (120-count) are currently being recalled nationwide by Haleon US Holdings LLC. The recall was issued due to incomplete inactive ingredient information on the exterior carton labeling, though the active medication is completely safe and unaffected.
