2,229 recalls tagged with “stop use immediately”.
Belkin is recalling its MMA008 charging stand and BPB002 and PB0003 power banks sold at multiple retailers due to a fire and burn hazard. The lithium-ion battery can overheat. Consumers should stop using the recalled devices immediately and contact Belkin for a full refund or store credit.
Shantou Chenghai Xingzigu Toy Industry recalled Bettina Doll Sets sold on Amazon after finding the unicorn’s battery compartment is easily accessed by children. Button cell batteries can cause serious injuries or death if swallowed. Stop using the recalled toys and request a full refund by emailing bettinaaftersales@outlook.com.
Jeni's Splendid Ice Creams recalls Passion Fruit Dreamsicle Ice Cream Bars for undeclared wheat and soy allergens. The recall covers 3,767 cases distributed to 10 states. Consumers should not eat the product and should seek a refund or replacement via email.
Microbiologics recalled 5 KWIK-STIK quality control kits for culture media after发现 some kits labeled for lot 818-111-7 were packed in pouches marked as lot 857-53-10. The mislabeling could affect quality control results for Vibrio parahaemolyticus tests derived from ATCC 17802. Laboratories and healthcare facilities should stop using the kit and follow the manufacturer’s recall instructions.
Nissan North America recalls 2025 Kicks vehicles due to a Shift-to-Park warning that may not activate when the vehicle is shut off in a gear other than Park. The recall targets 2025 Nissan Kicks. Nissan will reconfigure the BCM to activate the warning at no cost. Notifications began January 29, 2025, with more letters expected May 7, 2025.
Walgreens Saline Nasal Spray With Xylitol, distributed by Walgreens Co., is recalled nationwide. The product was found with microbial contamination, specifically Pseudomonas lactis, in a non-sterile formulation. Consumers should stop using the product immediately and contact Medical Products Laboratories, Inc. for guidance or consult a clinician.
Stryker recalled 320 units of the CranialMask Tracker on November 12, 2025, due to software errors during surgery. The device fails to activate properly, displaying an error message that prevents its use. Healthcare providers must stop using this device and follow recall instructions immediately.
Genepro Protein recalls 250 bags of its Whey 4th Generation Plasma Treated Protein sold nationwide after labeling failed to declare milk as an allergen. The product is mislabeled and could pose a risk for people with milk allergies. Consumers who purchased this product should not consume it and should email Genepro Protein, Inc. for refund or replacement information.
Olympus Corporation of the Americas recalled the Inner Sheath Model No. A2660 on November 11, 2025. Complaints of the ceramic tip breaking prompted the recall of nine units distributed nationwide. Patients and healthcare providers must stop using the device immediately.
Olympus Corporation of the Americas recalled 6,949 units of its Resection Inner Sheath on November 11, 2025, after reports of the ceramic tip breaking. This device, used in urologic applications, poses a high hazard risk. Healthcare providers and patients should stop using the device immediately.
Olympus Corporation of the Americas recalled 1,141 units of the Inner Sheath, Model No. WA22017T, on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately and follow the manufacturer’s instructions.
Olympus Corporation of the Americas recalled 437 units of the Inner Sheath, Model No. WA22017A, on November 11, 2025. The recall follows complaints of the ceramic tip breaking during use, posing a significant risk to patients. Healthcare providers and patients should cease use immediately and follow the manufacturer’s instructions.
Olympus Corporation recalled the Resection Sheath, Model No. A2666, on November 11, 2025, following complaints of the ceramic tip breaking. The recall affects one unit distributed nationwide in the U.S. Healthcare providers and patients must stop using the device immediately.
AVID Medical recalled 132 units of its Organ Recovery Kit on November 11, 2025. The devices are not suitable for organ transplant, posing a high risk to patients. Healthcare providers and patients should stop using the device immediately and follow recall instructions.
Olympus recalled its Inner Sheath, Model No. A2642, on November 11, 2025, due to safety complaints. Users reported the ceramic tip of the resection sheath breaking during use. This recall affects urological applications and poses a high risk to patients.
Olympus Corporation of the Americas recalled 118 units of its 28 Fr. resection sheath on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a risk of injury. Healthcare providers and patients must stop using the device immediately.
Olympus Corporation recalled 29 units of its Resection Sheath on November 11, 2025. The recall affects model numbers A22014A and A22014T due to complaints of the ceramic tip breaking. The company advises immediate cessation of use and adherence to recall instructions.
Olympus Corporation of the Americas recalled the Inner Sheath 21 Fr., Model No. A2660T, on November 11, 2025. The recall follows reports of the ceramic tip breaking during use. Patients and healthcare providers should stop using the device immediately.
Olympus Corporation of the Americas recalled 3,484 units of the Resection Sheath Model No. A22041A on November 11, 2025. Reports indicate the ceramic tip of the device may break during use, posing a serious hazard to patients. Healthcare providers and patients must stop using the device immediately and follow recall instructions.
Olympus Corporation of the Americas recalled 207 units of its Resection Sheath, Model No. A22043T, on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a serious hazard. Patients and healthcare providers must stop using the device immediately.