2,153 recalls tagged with “stop use immediately”.
Cipla USA, Inc. recalled 15,744 bottles of Cinacalcet Hydrochloride Tablets on November 14, 2025. The recall follows the discovery of a nitrosamine impurity exceeding acceptable daily intake limits. Consumers should stop using the product immediately and consult healthcare providers.
American Nuts recalls 2,700 units of Dry Roasted Macadamia Nuts, Unsalted Halves distributed to two consignees in Hawaii after a potential Salmonella contamination. The product has UPC 8 60011 44301 8 and Lot Code 307HMNC25L3. Stop consuming the product and contact American Nuts, LLC by telephone for a refund or replacement.
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.
Great Lakes Wholesale International recalled Great Lakes Select Battery Packs sold by multiple wholesalers nationwide. The packaging lacks child-resistant features for button cell and coin batteries. Stop using the packs now and contact the company for a full refund.
Tesla recalls Powerwall 2 energy storage systems sold through Tesla.com and certified installers nationwide due to fire and burn hazards. The lithium-ion cells can stop functioning during normal use, causing overheating and possibly smoke or flame. Owners should stop using the system and contact Tesla for replacement options.
Lupin Pharmaceuticals recalled 32,736 vials of Ganirelix Acetate Injection on November 13, 2025. The recall follows the discovery of impurities in the drug. Consumers and healthcare providers should stop using the product immediately to avoid health risks.
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.
Trek and Electra recall certain bicycles and replacement rear wheels sold by Trek authorized retailers and Trek.com due to a crash hazard. The coaster brakes can fail to engage, increasing the risk of loss of rider control. Consumers should stop riding recalled bikes, check serial numbers starting with WTU located under the bottom bracket, and contact a Trek or Electra dealer to schedule a free, 3
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.
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.
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.
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 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 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 of the Americas recalled 7,426 units of the A22040T resection sheath on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a high hazard to patients. Healthcare providers and patients 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 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.