527 recalls tagged with “adult product”.
LEACHOI recalled its adult portable bed rails on October 23, 2025, due to serious entrapment and asphyxiation hazards. The recalled product violates mandatory safety standards for bed rails and poses a high risk of injury or death. Consumers should stop using the bed rails immediately and seek a full refund.
Sauna360 recalled Tylö Halmstad and Kiruna Hybrid saunas on October 23, 2025, due to a fall hazard. The recalled products include models with potential bench collapse issues. Consumers should stop using the saunas immediately and contact the manufacturer for repairs.
Olympus Corporation of the Americas recalled the Thunderbeat surgical device on October 22, 2025, due to reports of adverse events. The recall affects 30 units distributed worldwide, including the US, Canada, and Japan. Patients and healthcare providers must stop using the device immediately.
Olympus Corporation of the Americas recalled the Thunderbeat, 5 mm, 45 cm, Pistol Grip device on October 22, 2025. The recall affects 30 units distributed worldwide, including the U.S., Canada, Brazil, Germany, Mexico, and Japan. Patients and healthcare providers must stop using this device immediately due to reports of adverse events.
Olympus Corporation of the Americas recalled the Thunderbeat 5 mm, 35 cm, Front-Actuated Grip on October 22, 2025. The recall follows reports of adverse events associated with the device. Healthcare providers and patients must stop using this product immediately.
123Herbals LLC recalled SILINTAN 25-pill bottles sold nationwide in the United States after FDA analysis found undeclared meloxicam. An NDA/ANDA violation is cited. Consumers and healthcare providers should stop using this product immediately and contact 123Herbals LLC for guidance.
Super Wheels recalled Vaast A/1 bicycles on October 16, 2025, after discovering a fall hazard. The recall affects 35 bicycle models and 15 frames sold in various colors. Consumers should stop using the bicycles immediately and contact the company for a replacement.
M.C.I. Foods recalled 1,040 cases of Egg and Cheese Breakfast Burritos on October 16, 2025. Testing revealed potential Listeria Monocytogenes contamination in the cooked egg ingredient. The affected products are not for retail sale and were distributed to institutional clients nationwide.
Yamaha recalled model year 2021-2025 golf car vehicles due to a crash hazard. The recall affects approximately 50,000 units sold nationwide since June 2020. These vehicles lack stop lights, posing a risk of serious injury or death.
Nat's Nuts LLC recalled 600 units of Cinnamon Whiskey Pecans on October 16, 2025. The product contains undeclared cashews, posing a serious allergy risk. The recall affects consumers in nine states, including New York and Florida.
Textron E-Z-GO recalled personal transportation vehicles due to a fire hazard. The recall affects RXV Freedom and Valor models from 2020 to 2025. Consumers should stop using these vehicles immediately.
Sugared+Bronzed recalled 2,090 tubes of Tinted Mineral Sunscreen SPF 50 on October 10, 2025. The recall stems from current Good Manufacturing Practice deviations. Consumers should stop using the product immediately and seek guidance.
VitaTienda Co U.S.A. recalled 3,295 bottles of Elixir by Coco March Mineral Sunscreen SPF 50 on October 10, 2025. The recall stems from CGMP deviations that could affect product safety. Consumers should stop using the sunscreen immediately and contact their healthcare provider for guidance.
CA BOTANA recalled 555 tubes of Doctor D. Schwab Controlling Balm on October 10, 2025, due to CGMP deviations. The affected product contains salicylic acid and tea tree oil. Consumers should stop using the balm immediately and contact CA BOTANA International for guidance.
Major Pharmaceuticals recalled Gabapentin Capsules, USP, 100 mg, on October 10, 2025, due to failed impurities specifications. The recall affects several lot numbers distributed nationwide. Consumers must stop using the affected capsules immediately.
Lannett Company, Inc. recalled 46,848 bottles of Niacin Extended-release Tablets on October 10, 2025. The recall follows reports of failed dissolution specifications, which could affect medication effectiveness. Consumers should stop using the product immediately and consult healthcare providers for guidance.
Doctor D. Schwab recalled 805 tubes of Shimmery Sun Lotion Sunscreen SPF 30 on October 10, 2025. The recall follows significant deviations from current good manufacturing practices (CGMP). Consumers should stop using the product immediately and contact CA BOTANA for guidance.
CA Botana International recalled 1,167 tubes of Doctor. D. Schwab Mineral Sunscreen SPF 50 on October 10, 2025. The recall stems from current good manufacturing practices (CGMP) deviations. Affected products include Lot Code D54596 with an expiration date of January 31, 2028.
CA Botana International, Inc. recalled 874 tubes of Ultra Umbrella Sunscreen SPF 30 on October 10, 2025. The recall stems from CGMP deviations that may affect product safety. Consumers in CA, CO, FL, PR, and WA should stop using the product immediately.
Advanced Pharmaceutical Technology recalled 22,843 cartons of TESTO-100 CIII testosterone pellets on October 3, 2025. The recall follows a risk of microbial contamination that could compromise product sterility. Consumers and healthcare providers should stop using the product immediately and seek guidance.