24 recalls tagged with “teen product”.
BMW recalls 2025-2026 X1 and X2 models plus MINI Cooper and Countryman variants for front seat belt retractors with damaged torsion bars. The defect may fail to restrain occupants in a crash. Dealers will replace both front retractors at no cost. Owner letters begin November 7, 2025. VIN lookup will be available on NHTSA.gov the same day.
SpringFlower recalls 5-in-1 Montessori Toy Sets sold on Amazon after a choking hazard is identified in an airplane-shaped teething toy. The recall targets model SFTODD05IN1. Consumers should stop using the set immediately and contact SpringFlower for a refund or replacement.
Fagron Compounding Services recalled 34,260 bags of Vancomycin HCI Injection across the United States. The recall cites lack of sterility assurance and a blue Break-Off-Part that could detach from the administration port. Healthcare providers and patients should stop using the product immediately and follow manufacturer guidance.
Cook Incorporated recalls Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set after lots were labeled with expiration dates that exceed true shelf life. The recall affects two reference parts with multiple UDI and lot numbers. Healthcare facilities should stop use and follow recall instructions.
Cook Medical recalled 75 CTO-18 Micro Wire Guide devices distributed worldwide. The recall cites expiration date labeling that exceeds the true shelf life. Healthcare providers should stop using affected lots immediately and follow manufacturer instructions.
Cook Medical recalled 49 units of the Approach CTO-12 Micro Wire Guide due to expiration dates that exceed the true shelf life. The recall covers two reference part numbers and multiple lots distributed worldwide. Healthcare providers and patients should stop using the affected devices immediately. Follow the manufacturer’s recall instructions or contact a healthcare provider for guidance.
Cook Medical recalled the Thal-Quick Chest Tube Tray, reference part number C-TQTSY-3200, Order G07242, due to expiration dates that exceed true shelf life. The recall is active and worldwide. The hazard is labeling that misstates shelf life. Patients and healthcare providers should stop using the affected devices immediately and follow Cook’s recall instructions.
Philips is recalling 798 Azurion 3 M15 systems worldwide, including 42 units in the United States. The wired foot switch may fail to initiate X-ray imaging or fail to produce consistent imaging. Healthcare providers should stop using the affected devices and follow recall instructions issued by Philips.
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.
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.
Exactech recalls 596 Equinoxe Core Instrument Kit units due to a missing cross-pin on the impacter handle. The alert, categorized as a Class II recall, was issued Feb 3, 2026 and remains active. Affected kits were distributed across the United States and in multiple international markets. Stop using the device and follow manufacturer instructions for recall remedies.
Instrumentation Laboratory recalls 8 GEM Premier 5000 cartridges worldwide after PCSND warm-up errors cause GEM PAK ejections. The defect may prolong turnaround times and delay results. Hospitals and clinics should stop using the device and contact the manufacturer for instructions.
Instrumentation Laboratory recalls 489 GEM Premier 5000 PAK cartridges worldwide after reports of Process Control Solution Not Detected errors during warm-up. iQM2 monitors the testing process and may allow continued use after AutoPAK Validation. The recall highlights potential operational disruptions in patient management.
Waldemar Link GmbH & Co. KG recalls 4 Endo-Model Replacement Plateau units worldwide, including the US state of New Jersey. A longitudinal fracture can detach the bushing from the screw shaft. Stop using the device and follow the manufacturer’s recall instructions.
Luyuan recalls two youth ATVs for a crash hazard that could cause serious injury or death. The models are X-Pro Eagle 40cc Youth ATV, CARTOONS, and FRP Sahara 40cc Youth ATV, SHR 40-RED-M. Consumers should stop using the ATVs immediately and contact Luyuan for a free repair.
Laiwu Manhing Vegetables Fruits Co recalled 245 cartons of irradiated onion granules sold in California after foreign objects were found in the powder. The contamination is described as black plastic planting film. Consumers should not consume the product and should contact the company for refund or replacement via email.
B Braun Medical Inc recalled 13,600 extension set units used with Infusomat Space and related pumps sold through multiple healthcare distributors worldwide. The recall cites a backflow risk from secondary piggyback containers into primary IV containers and an inability to prime due to occlusion. Healthcare providers and facilities should stop using the device immediately and follow manufacturer-re
B Braun Medical recalled 1,200 extension sets used with Infusomat Space large-volume pumps distributed worldwide to hospitals and clinics. The recall cites potential backflow from secondary IV containers into primary containers and an inability to prime (occlusion). Healthcare facilities should stop using the devices immediately and follow the recall instructions issued by the manufacturer.
Beauty4Pros LLC recalls Karina Daily Moisturizer SPF 25 distributed to CA, CO, FL, PR, WA after CGMP deviations. 1,492 tubes affected. Stop use immediately and contact CA Botana International for guidance.
Wholesale Produce Supply LLC recalled 307 cases of cantaloupe chunks sold under Fresh & Finest, Harvest Cuts and other labels. The recall targets a broad range of container sizes and UPCs in IA, IL, ND, NE and WI. The recall cites potential Listeria monocytogenes contamination and is classified as Class I.