125 recalls tagged with “laceration risk”.
Head USA recalls ski boots with fluorescent yellow components from 2016–2022 model years. The recall covers boots and inserts with six-digit article codes. Consumers should stop using recalled boots immediately and contact Head for a free replacement or sole-insert option.
Amazon recalled the Amazon Basics Camping Folding Pocket Knife sold by Amazon after a laceration hazard was identified. The knife has a 3.5-inch blade. The folding mechanism can fail to remain securely closed, posing a risk of serious cuts.
Chiesi USA recalled 7,235 Curosurf vials distributed nationwide to hospitals and clinics. The recall cites a lack of assurance of sterility. Healthcare providers should stop using the product immediately and contact Chiesi USA for guidance.
Western Mixers Produce & Nuts recalled 384 cases of First Street Chilli Spanish Peanuts after a glass fragment was found inside sealed containers. The recall covers two consignees and 53 retail locations nationwide. Consumers should not eat the product and should email the company for refund or replacement.
JFE FRANCHISING INC recalled two dumpling products sold at retailers nationwide: Dumpling Vegetable 4.5 oz (UPC 011110658067) and Loaded Dumpling Vegetable 5.7 oz (UPC 011110696953) due to a glass contamination risk. The recall is Class II with a high hazard level. Consumers should not eat the dumplings and should contact JFE FRANCHISING INC by email for refund or replacement.
JFE Franchising Inc. recalls Dumpling Party Tray products and a Cheetos Flamin Hot Loaded Dumpling item after glass fragments were found in the trays. The FDA enforcement report lists glass as the foreign object hazard. Consumers should not eat these products and should seek refunds or replacements via email.
Ajinomoto Foods North America recalled Trader Joe's Vegetable Fried Rice sold at Trader Joe's nationwide after glass fragments were found in the product. The contamination involves glass shards ranging from 1 to 3 cm long and 2 to 4 mm wide. Consumers should not eat this product and should contact Ajinomoto Foods North America for refunds or replacements.
Ajinomoto Foods North America recalls Ajinomoto Golden Tiger Vegetable Fried Rice sold at multiple retailers nationwide. Glass fragments measuring 1-3 cm long and 2-4 mm wide have been found in frozen rice. Consumers should not eat the product and should contact Ajinomoto for refunds or replacements.
Ajinomoto Foods North America recalled 9,913 cases distributed nationwide after glass fragments were found in Tai Pei Shrimp Fried Rice. The glass pieces measure 1-3 cm long and 2-4 mm wide. Consumers should not eat the product and should contact Ajinomoto for refund or replacement information.
Ajinomoto Foods North America recalled 35,955 pounds of Ajinomoto Japanese-Style Vegetable Fried Rice distributed by multiple retailers in 43 states after glass fragments were found in the product. The glass pieces measure 1 to 3 cm long and 2 to 4 mm wide. Consumers who bought the product should not eat it and should contact Ajinomoto Foods North America for a refund or replacement.
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.
Ajinomoto Foods North America recalled 109,741 cases of Kroger Chinese Inspiration Vegetable Fried Rice sold at Kroger stores after glass fragments were found. Glass pieces measure 1 to 3 cm long and 2 to 4 mm wide. Consumers should not eat this product and should seek a refund or replacement from Ajinomoto Foods North America.
Ajinomoto Foods North America recalls 537,033 pounds of Ajinomoto Green Gyoza Vegetable & Edamame Dumplings sold nationwide after glass fragments were found. Glass pieces range from 1 to 3 cm long and 2 to 4 mm wide. Consumers should not eat the recalled dumplings and should contact Ajinomoto Foods North America for a refund or replacement.
Philips Medical Systems Nederland B.V. recalls 8 Allura Xper FD20/15 OR Tables worldwide due to a risk that X-ray imaging may not start or may stop intermittently when using the wired foot switch. The issue is tied to System Code 722059 and requires immediate action. Hospitals and patients should stop using the device and follow the manufacturer’s recall instructions.
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
Civco Medical Instruments Co. is recalling 5 eTRAX Needle Sensor 14G units for Aurora Trackers. The recall cites a programming and inspection error that could cause the needle tip position to be misidentified on the user interface. Stop using the device immediately and contact Civco for instructions.
Joyreal recalled busy board toys on February 26, 2026, due to choking and laceration hazards. The toys can have small parts that pose serious risks to children. Consumers must stop using these toys immediately and seek refunds.
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.
Olympus Corporation of the Americas is recalling 106 Everest Bipolar Cutting Forceps worldwide. The devices can have welding defects that may cause the jaw to break during use. Stop using immediately and contact Olympus or your healthcare provider for instructions.
Synthes recalls 77 bone taps nationwide after a lot swap created an incorrect thread. The recall covers the 2.4 volt locking screw tap to 90mm, part number 03.424.124-US. Healthcare providers and facilities should stop using the device immediately and follow recall instructions.