269 recalls tagged with “metal”.
Fourour Kiddies recalled tip restraint kits after tests found plastic components could break, creating a tip-over risk. The recall affects kits used to secure furniture to walls. Consumers should stop using the recalled restraints and seek a stainless steel replacement from 4our Kiddies.
Bioenrrty recalled MPINOI branded adult portable bed rails sold on Amazon after reports of serious entrapment and potential asphyxiation. The recall cites a violation of a mandatory standard and missing hazard warnings. Consumers should stop using the product immediately and seek a full refund.
Nexgrill recalls more than 10.2 million metal wire bristle grill brushes sold at Home Depot. Bristles can detach and stick to food or grills. Consumers should stop using recalled brushes and contact Nexgrill for a full refund issued as a gift card.
Petzl America recalls Nomic and Ergonomic ice climbing axes due to a shaft break risk that could cause a fatal fall. The recall involves specific serial ranges across two models and targets accessories sold through specialty retailers and online shops. Consumers should stop using the axes and pursue a free repair kit from Petzl America.
Goregent is recalling Goregent-branded infant walkers sold on Amazon. The recalled walkers can fit through a standard doorway and fail to stop at the edge of a step. Parents should stop using the recalled walkers immediately and contact Goregent Official Store for a full refund.
Tainoki Fine Furniture recalled three office chairs sold at HomeGoods stores nationwide from August 2025 through December 2025 for about $180 to $200. The base can bend, creating a fall hazard. Stop using the chairs immediately and follow the recall instructions on the company site for a full refund.
Specialized recalled all Turbo Como SL electric bicycles sold online at specialized.com and through Authorized Specialized Retailers. A fatigue crack in the fork steerer tube can cause progressive fork failure and a fall. Owners should stop riding immediately and arrange a free fork replacement at an Authorized Dealer; replacement parts are expected in Spring 2026.
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.
Straumann USA recalled 13 Custom Abutment Ti RC units distributed worldwide, including the United States and Canada. A TAN material was misidentified as Titanium Ti Gr4 D during manufacturing, causing RC Titanium abutments to be made from TAN material. Clinics and patients should stop using the devices immediately and follow recall instructions from Straumann USA or their healthcare providers.
Straumann USA LLC recalls 7 Custom Abutment AS Ti for Straumann RC. The recall follows a material mix-up during manufacturing. A TAN material bar was incorrectly identified as Titanium Bar Ti Gr4 D, causing RC Titanium abutments to be made with TAN material. Stop using the device and contact Straumann for instructions immediately.
Lucerne recalled 12,222 tubs of 2% cottage cheese sold at Albertsons stores after metal fragments were found in packaging. The object is a curled stainless steel spring and could end up in the product. Stop using the product and contact Albertsons Companies LLC for a refund or replacement.
Nuts.com recalled 10,190 pounds of Espresso Malted Milk Balls distributed nationwide in the United States. The recall cites undeclared wheat and soy allergens from soy lecithin in the ingredient statement. Consumers who bought this product should not consume it and should contact Nuts.com for a refund or replacement via email.
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.
Philips Medical Systems Nederland B.V. recalled 5,084 ALLURA Xper FD20 imaging systems sold nationwide and internationally after finding that the wired foot switch may fail to initiate X-ray imaging or perform intermittently. The defect can delay or interrupt imaging during patient care. Healthcare facilities should stop using the devices and follow the manufacturer’s recall instructions.
Philips recalled 85 Allura Xper FD20/10 imaging systems distributed nationwide and internationally. The devices may fail to initiate X-ray imaging or do so intermittently when using the wired foot switch. Hospitals and clinicians should stop using the device and follow the manufacturer’s recall instructions.
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.
Rising Pharmaceuticals recalls 1,200 Temozolomide 5 mg capsules nationwide after a stability test found out-of-spec impurities. The drug is Rx-only, with NDC 16571-816-51 and lot 1TM0524003A. Stop using immediately and contact a healthcare provider for guidance.
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.
Civco Medical Instruments Co. recalled 21 eTRAX Needle Sensors for Aurora Trackers sold to healthcare providers in Ohio, Pennsylvania and Washington. The devices have an inspection and programming error that can cause the needle tip position to be misidentified on the user interface. Clinicians should stop using the devices immediately and follow recall instructions from Civco.