Browse through 2,970 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Olympus Corporation of the Americas recalled 88,268 units of the Thunderbeat surgical device on October 22, 2025. The recall follows reports of adverse events associated with the device. Healthcare providers and patients should stop using the device immediately and follow the recall instructions.
Olympus Corporation of the Americas recalled the Thunderbeat 5 mm, 35 cm, Front-Actuated Grip on October 22, 2025. The recall follows reports of adverse events associated with the device. Healthcare providers and patients must stop using this product immediately.
Medtronic MiniMed recalled 12,126 CareLink Clinic units worldwide after a software error misdisplays the 24-hour Sensor Glucose Overview Graph. The faulty software could prompt clinicians and patients to make therapy decisions based on incorrect glucose data. Patients should stop using the device immediately and contact Medtronic MiniMed or their healthcare provider for instructions.
Bristol-Myers Squibb recalled 12,778 Opdualag single-dose vials nationwide after a lack of assurance of sterility was identified. The product is nivolumab and relatlimab-rmbw injection. The recall date is 2025-10-21. Healthcare providers should stop using affected lots and follow the recall letter guidance.
Mindray DS USA recalled 54 Isoflurane V90 Vaporizers used with the A9 Anesthesia System, distributed worldwide to healthcare providers. The devices have a potential for anesthesia leakage. Clinicians should stop using immediately and contact Mindray DS USA for instructions.
Mindray DS USA recalled 148 Sevoflurane V90 electronic vaporizers used with the A9 Anesthesia System. The devices have a potential for anesthesia leakage. Healthcare facilities should stop using the device immediately and follow manufacturer instructions.
123Herbals LLC recalled SILINTAN 25-pill bottles sold nationwide in the United States after FDA analysis found undeclared meloxicam. An NDA/ANDA violation is cited. Consumers and healthcare providers should stop using this product immediately and contact 123Herbals LLC for guidance.
Straumann USA recalled 61 Emdogain demonstration devices distributed nationwide in 10 states. The devices, intended for demonstration only, could be placed in patients. Healthcare providers and patients should stop using immediately and follow recall instructions from Straumann for disposal or replacement.
Town Food Service EQ CO Inc. recalled approximately 11,300 aluminum sauce pans on October 17, 2025, due to leachable lead levels. Consumers should not use these pans and should seek refunds or replacements. The recall affects various sizes sold across multiple states and locations in Canada.
M.C.I. Foods recalled 1,040 cases of ready-to-eat Egg and Cheese Breakfast Burritos and Wraps sold to seven distributors nationwide for institutional use. A cooked egg ingredient used in the ready-to-eat products tested positive for Listeria monocytogenes. Consumers should not consume the product and should contact M.C.I. Foods for refund or replacement; notification will be by letter.
iFIT recalls NordicTrack Rowing Machines with model numbers NTRW19147.0, NTRW19147.1, NTRW19147.2 and NTRW19147.3. The screen console can overheat and ignite, creating a fire hazard. Stop using the machines immediately and unplug them; contact iFIT for a free console replacement.
RH recalled Byron tables and desks sold at RH Galleries and outlets and on RH.com from November 2023 through July 2025. The recall covers 31 SKUs across three models with stone and marble tops and wood legs. The recalled furniture can collapse if a gap forms between the leg and tabletop and a horizontal force is applied. Consumers should stop using recalled units and contact RH for a full refund,,
M.C.I. Foods recalled 330 cases of Cheese and Egg with Green Salsa Breakfast Burrito sold to seven distributors nationwide. The ready-to-eat burrito contains a cooked egg ingredient that tested positive for Listeria monocytogenes. Consumers should not eat the product and should contact M.C.I. Foods for refund or replacement by letter.
Belivium recalled its baby loungers sold on Amazon after safety concerns tied to suffocation and entrapment hazards. The loungers have a foam sleeping pad and padded bumpers with a cloth cover. Parents should stop using the loungers immediately and contact Belivium for a full refund.
Wilteexs recall 1-liter bioethanol fuel bottles imported by Wilteexs after safety-standard violations. The bottles lack flame mitigation devices and carry a false “Non Toxic” disclaimer. Consumers should stop using the recalled bottles and contact Wilteexs for a full refund.
WLIVE recalled its Fabric 12-Drawer Dressers sold on Amazon after identifying a serious tip-over and entrapment hazard. The dressers are unstable if not anchored to the wall, violating the mandatory standard for clothing storage units under the STURDY Act. Consumers should stop using the recalled dressers immediately and contact WLIVE for a full refund.
DEVI brand Cinnamon Powder, imported and distributed by Homeneeds Inc. in Bellevue, WA, is recalled after FDA testing found lead at 2.92 mg/kg. The recall covers 7 cases and about 140 packets. Consumers should not consume the product and contact Homeneeds for a refund or replacement.
Textron E-Z-GO recalled certain personal transportation vehicles due to a fuel-line leak that can spark a fire. The recall covers RXV Freedom and Valor PTVs from model years 2020-2025 and TXT Freedom and Valor PTVs from model years 2020-2022. Dealers will inspect and replace the fuel line at no cost, and owners should stop using the vehicles until inspected.
AOWOS recalled approximately 42,000 12-drawer dressers sold on Walmart.com due to a tip-over hazard. The dressers lack stability if not anchored to the wall, posing serious risks of injury or death to children. Consumers should stop using the dressers immediately and contact AOWOS for a full refund.
Super Wheels Inc. recalled Vaast A/1 bicycles and framesets sold through retailers after a fall risk was identified. The frame can develop a hairline fracture near a weld, which can cause the tubes to separate. Owners should stop riding immediately and contact Super Wheels for a free replacement frame and up to $200 for a bike-shop rebuild.