527 recalls tagged with “adult product”.
Acme United recalled FIRST AID ONLY Hand Sanitizing Wipes, 1,000 wipes per case, nationwide in the United States, on 2026-01-20. The action follows CGMP Deviations cited by the maker. Stop using the wipes and contact Acme United for guidance.
Acme United Corporation recalled Med Nap BZK Antiseptic Towelettes, 100-count, distributed nationwide. The FDA-listed CGMP deviations raise concerns about manufacturing quality and product safety. Consumers and healthcare providers should stop using the product and follow the recall letter for guidance.
Dynarex recalled 100-pack BZK Antiseptic Towelettes sold nationwide after FDA enforcement cited CGMP deviations. The recall covers multiple lots, including Lot 52347-R, 52348-R, 52349-R, 52350, 52351-R, 52352, Exp. Date Mar 2027 and Exp. Date Jun 2027. Consumers should stop using the product immediately and contact ACME UNITED CORPORATION or their healthcare provider for guidance.
ACME UNITED recalled Max Packaging Antibacterial Towelette nationwide in the United States after CGMP deviations were identified. Manufacturing quality deviations prompted the recall, classified as Class II and labeled as high hazard. Stop using the product immediately and contact ACME UNITED CORPORATION or your healthcare provider for guidance.
ACME United Corporation recalled 212,607,900 First Aid Only BZK Antiseptic Towelettes sold nationwide. The recall cites CGMP deviations in manufacturing. Consumers should stop using the product immediately and contact ACME United Corporation for guidance.
Nationwide recall of Dukal BZK Antiseptic Towelettes due to CGMP deviations. The products are manufactured for Dukal, LLC in Ronkonkoma, NY and distributed across the United States. Stop using immediately and contact ACME United Corporation for guidance.
R.X.Y recalled adult bicycle helmets on January 15, 2026, due to safety violations. The helmets fail to meet mandatory impact standards, posing a serious risk of injury or death. Consumers should immediately stop using the helmets and seek a refund.
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.
Aesculap recalls 126 MINOP TROCAR 150MM devices distributed nationwide to U.S. hospitals and clinics after regulators flagged a shaft length issue. The shaft may be longer than specified, potentially harming tissue during procedures. Healthcare facilities should stop using the devices and follow manufacturer recall instructions immediately.
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.
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.
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.
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.
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.
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.
Volkswagen Group of America recalled certain 2025 Tiguan vehicles due to a loose tie rod bolt. This condition may lead to a loss of vehicle control, increasing crash risk. Owner notification letters were mailed on September 5, 2025.
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 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.
Karison Foods & Snacks recalled 2,760 units of Besan Laddoo on January 6, 2026. The product contains undeclared milk, posing a serious risk to consumers with dairy allergies. The recall affects distribution in New York, New Jersey, and Virginia.