448 recalls tagged with “poisoning risk”.
Ajinomoto Foods North America recalled 8,097 cases of Ajinomoto Vegetable Gyoza Dumplings sold nationwide through retailers. Glass fragments measuring 1 to 3 cm long and 2 to 4 mm wide were found in the product. Consumers should not eat the dumplings and should contact Ajinomoto Foods North America for refund or replacement.
K.C. Pharmaceuticals recalled 315,144 sterile eye drop bottles distributed nationwide after lack of sterility. The products span several brands including GNP Eye Drops Redness and Dry Eye Relief, Leader Eye Drops Redness Relief, and Foster & Thrive Redness Relief Eye Drops. Consumers should stop using the products immediately and follow guidance from KC Pharmaceuticals or their healthcare provider
4,611 bottles are recalled nationwide. The product is Savannah Bee Company Honey BBQ Sauce Mustard, distributed to numerous states. The bottle actually contains Honey BBQ Sauce 'Sweet' which contains wheat and soy not declared on the Mustard label. Stop using the product and contact Savannah Bee Company for a refund or replacement.
American Laboratories recalled 468 kg of Pepsin 1:3000 Powder distributed through 11 wholesale accounts in the United States and one in Australia. The powder is potentially contaminated with Salmonella and could cause illness if used. Consumers who purchased this product should not consume it and should contact American Laboratories by email for refund or replacement.
American Laboratories recalled 370 kg of Pepsin 1:10,000 Powder sold through 11 wholesale accounts in AZ, CA, FL, MO, NM, OH, SC, UT, WI and one account in Australia after a potential Salmonella contamination. The product carries a possible Salmonella contamination risk. Consumers should not consume the product and should contact American Laboratories for refund or replacement via email.
American Laboratories recalled 400 kg of Pepsin Full Strength Powder sold to 11 direct wholesale accounts in AZ, CA, FL, MO, NM, OH, SC, UT, WI and one wholesale account in Australia after a recall cited potential Salmonella contamination. The product is Item #5000545 and packed in double poly-lined drums or boxes. Consumers should not consume this product and should contact American Laboratories,
Gooder Foods recalled 61,176 cartons of pasta on September 10, 2025, due to undeclared allergens. The product may contain cashews, posing a risk to consumers with nut allergies. The affected lots were distributed across multiple states in the U.S. and Canada.
Olympus Corporation of the Americas recalled 93 PKS Cutting Forceps worldwide due to welding defects that can cause the jaw to break during clinical use. The issue involves Model 3005PK and UDI 00821925036000. Action is required immediately and providers should follow recall instructions.
Imu-Tek Animal Health recalled 1,003 bottles of Colostrum-5 sold through various retailers in 30 states after determining the product may be under-processed. The under-processing could render the product unsafe. Consumers should not consume the product and should contact Imu-Tek Animal Health for refund or replacement.
Mei Heong Yuen Tangerine Flavor Roasted Peanuts, distributed in the United States by Super World Trading Inc., are recalled across 595 cases under H-0641-2026. The product contains cyclamate, a banned sweetener. Consumers should stop consuming the product and contact the distributor for refunds or replacements.
Joly's LLC recalled 80% Vinegar on February 19, 2026, due to serious risks of poisoning and chemical burns. The product lacks essential warning labels and first aid instructions, violating federal safety laws. Consumers should stop using the product immediately and seek a refund.
Kirkman recalled 178 bottles of MAXIMUM Zone 1 4% Lidocaine Cream distributed nationwide in the U.S. by Dermal Source. The recall cites stability data that does not support the stated expiry date. Consumers and healthcare providers should stop using this product immediately and contact Kirkman for guidance.
Cipla USA recalls 271 cartons of Nilotinib 150 mg capsules nationwide after stability tests show out-of-spec results. The issue affects description and appearance by visual inspection. Stop using and contact Cipla USA or a clinician for guidance.
Medline Industries, LP recalled 14,379 Airway Exam Kits containing Olympus biopsy valves nationwide. The recall cites rubber fragments detaching from the slit of single-use biopsy valves. Potential harm includes a foreign body in the patient’s tracheobronchial tree, inflammatory response, hypoxia, and longer procedures. Providers and patients should stop using the kit and follow recall directions.
Medtronic MiniMed recalled 29,074 Paradigm Real-Time insulin pumps worldwide. The devices may deliver insulin improperly when the pump is elevated or lowered relative to the infusion site due to gravitational effects. Patients should stop using the pumps immediately and follow recall instructions from the manufacturer and their healthcare provider.
Harbin Jixianglong Biotech Co. recalled semaglutide for Rx compounding use distributed nationwide to healthcare providers in the United States. The recall cites CGMP deviations and failure to complete process validation and bacterial endotoxin method validation before distribution. Healthcare providers and patients should stop using this product immediately and contact the manufacturer or their CL
Harbin Jixianglong Biotech Co. recalled Semaglutide for Rx compounding use nationwide in the United States. The recall cites CGMP deviations and failure to complete endotoxin validation before distribution. Healthcare providers and patients should stop using the product immediately and contact the company or a healthcare provider for guidance via email.
Oregon Potato Company recalled 55,689 pounds of IQF Blueberries on February 12, 2026, due to potential contamination with Listeria monocytogenes. The affected products include 30-pound cases and 1,400-pound totes distributed in Michigan, Oregon, Washington, Wisconsin, and Canada.
Burlington Medical recalled 51 Blocker devices sold worldwide after a recall notice. The devices may degrade attenuation over time, shortening their lifespan. Stop using the devices immediately and follow the manufacturer’s recall instructions. Contact Burlington Medical, LLC or your healthcare provider for guidance. Distribution is worldwide.
Waldemar Link GmbH & Co. KG recalls 74 Embrace Drill Tower devices distributed in 15 U.S. states. The recall notes mixed-up article numbers in the overview of the instruments. The surgical steps are correct. Stop using the device immediately and follow manufacturer instructions.