915 recalls tagged with “adult product”.
Live it Up brand recalled 795,834 units of Super Greens powder on January 15, 2026, due to possible Salmonella Typhimurium contamination. The affected products are sold nationwide, including Puerto Rico and Guam. Consumers should not consume the product and seek refunds immediately.
Aonic Inc. recalled 780 bottles of its Complete dietary supplement on January 15, 2026, due to potential contamination with E. coli and Pseudomonas aeruginosa. Consumers in Utah should stop using the product immediately and seek refunds or replacements. The recall affects specific lots with expiration dates of December 27, 2026.
KVK-Tech Inc. recalled 31,676 packages of Oxycodone Hydrochloride Tablets on January 14, 2026. Defective seals may cause tablets to fall out, posing a health risk. Customers should stop using the product immediately and seek guidance from healthcare providers.
Waldemar Link GmbH & Co. KG recalled 2 units of Endo-Model Replacement Plateau with Item Number 15-0027/11. The defect could cause the bushing to detach from the screw shaft after a longitudinal fracture. Health care providers and patients should stop using the device and await manufacturer instructions.
Waldemar Link GmbH & Co. KG recalls its Endo-Model Replacement Plateau implant. Three units are affected worldwide, including New Jersey in the United States. The defect allows a bushing to detach from the screw shaft after a longitudinal fracture. Healthcare providers and patients should stop using the device immediately and follow the manufacturer’s recall instructions. Notification was sent by,
Waldemar Link GmbH & Co. KG recalled 4 Endo-Model Replacement Plateau devices, Item Number 15-8030/12, sold to hospitals and clinics worldwide including New Jersey. The defect involves a plateau screw, where a longitudinal fracture could cause the bushing to detach from the screw shaft. Healthcare providers and patients should stop using the device immediately and follow recall instructions from/
Waldemar Link recalled 7 Endo-Model Replacement Plateau implants worldwide, including a NJ distribution. The defect could cause the bushing to detach from the screw shaft after a longitudinal fracture. Health providers should stop use and await recall instructions.
Waldemar Link GmbH & Co. KG recalls 8 units of Endo-Model Replacement Plateau worldwide after a reported risk that a bushing could detach from the screw shaft due to a longitudinal fracture. The recall also covers US distribution in New Jersey. Health authorities have classified the risk as high. Patients and healthcare providers should stop using the device immediately and follow recall guidance.
Medartis AG recalled the 2.5 TriLock Screw 16mm HD7, 1/Pkg, sold worldwide through medical distributors including the US states of Indiana and Pennsylvania. The recall stems from a mix-up between 2.5mm and 2.8mm outer diameter screws. Healthcare providers and patients should stop using the device immediately and follow manufacturer recall instructions.
Sangohe recalled adult portable bed rails on January 8, 2026, after identifying risks of serious injury and death. The bed rails can entrap users, leading to potential asphyxiation. Consumers should stop using the product immediately and seek a full refund.
Agrish recalled adult portable bed rails on January 8, 2026. The recall affects models 2512, 2513, and 2516 due to an entrapment hazard. Consumers should stop using the product and seek a full refund.
Medline Industries recalled 14,525 dialysis convenience kits on January 8, 2026. The recall affects multiple product SKUs due to potential silicone seal failures. These issues may cause therapy delays or exposure to contaminants.
Medline Industries recalled 31,848 dialysis dressing change kits on January 8, 2026. The recall follows reports of defective silicone seals on Tego Connectors that may occlude fluid paths. This defect can delay therapy and expose patients to biological contaminants.
Olympus Corp. of the Americas recalls 55 ShockPulse-SE Lithotripsy System units distributed internationally. Mis-wired component may create noise on the power supply and ultrasonic circuit. Hospitals and providers should stop using the device immediately and follow recall instructions. Notify Olympus or your healthcare provider for guidance.
Olympus Corporation of the Americas recalled 30,489 units of the Single Use 3-Lumen Sphincterotome V on January 7, 2026. The recall stems from devices that failed to undergo proper thermoforming, risking deformation and performance loss. Healthcare providers and patients must stop using the device immediately.
Olympus Corporation of the Americas recalled 1,072 units of its Disposable Triple Lumen Sphincterotome on January 7, 2026. The recall addresses devices that did not undergo proper thermoforming, risking performance failure. Healthcare providers and patients should stop using the devices immediately.
Ford Motor Company recalls 2025 F-250 SD and other SD models for a brake pedal pushrod retaining spring that may not be installed. The defect can cause a sudden loss of brake function and a crash risk. Owners should not drive the vehicle until repaired. Ford will inspect and repair the brake pedal assembly free of charge; letters were mailed June 20, 2025.
HerbsForever recalled 45 units of its Gastro Care Ayurvedic Herbal Supplement on January 6, 2026. The recall follows the discovery of a potential undeclared allergen, wheat, which poses a serious risk to consumers with wheat allergies. Affected products were sold online nationwide.
Herbs Forever recalled 45 units of Hingwastika Churna on January 6, 2026. The product may contain undeclared wheat, posing a health risk to consumers with wheat allergies. Customers should stop using the product immediately and contact the company for a refund or replacement.
Karison Foods & Snacks Inc. recalled 2,760 units of its Panjiri snack on January 6, 2026. The product contains milk, which is not declared on the label. This recall affects consumers in New York, New Jersey, and Virginia.