989 recalls tagged with “adult product”.
Gold Star Distribution recalled toothbrushes and toothpaste on December 26, 2025, due to potential rodent exposure. The recall affects products distributed nationwide, particularly in Minnesota. Consumers should stop using these items immediately and follow recall instructions.
Gold Star Distribution is recalling Tylenol products distributed nationwide. The recall concerns CGMP deviations and insanitary conditions at the distributor’s facility. Consumers should stop using these Tylenol products immediately and contact Gold Star Distribution for guidance.
Medline Industries, LP recalled 141,971 suction catheter kits on December 24, 2025. The kits may contain a smaller catheter that can lead to serious respiratory issues. Health providers and patients must stop using the kits immediately to prevent potential harm.
Zimmer Surgical recalled 51 A.T.S. 3200TS Tourniquet Systems on December 24, 2025, due to a malfunctioning user interface. The device may freeze or become unresponsive in non-English language settings, risking delays in emergency situations. Healthcare providers should stop using the device immediately and follow recall instructions.
B.C. Williams Bakery Service recalled 720 bags of Bread and Roll Mix on December 23, 2025. The recall stems from the undeclared milk allergen, posing a high risk to consumers. The affected products were distributed nationwide.
Willy Pete's Chocolates recalled 54 units of Almond Despair dark chocolate on December 22, 2025. The product contains undeclared almonds which pose a risk to consumers with nut allergies. Customers should stop using the product and seek a refund or replacement.
HANDELNINE GLOBAL recalled Rheumacare capsules on December 22, 2025, after discovering lead contamination. The recall affects four bottles of 30 capsules each distributed in New York. Consumers should stop using the product immediately and contact their healthcare provider.
ICU Medical has recalled over 14 million needle-free access devices after reports of fluid leaks and potential exposure to biological contaminants. The recall affects devices distributed worldwide, including in 50 states and multiple countries. Users must stop using these devices immediately and follow recall instructions from the manufacturer.
Boston Scientific recalled 59 AXIOS Stents on December 19, 2025. Increased reports of deployment and expansion issues pose serious risks during procedures. Users should stop using the devices immediately and follow recall instructions.
Sato Pharmaceutical Co., Ltd. recalled 3,640 bottles of INON ACE Antacid tablets on December 19, 2025. The recall follows failed disintegration specifications, indicating the tablets may not dissolve properly. Consumers should stop using the product immediately and seek guidance from healthcare providers.
Bisaf Strep A Self-Test from Altruan GmbH remains active in recall status after the FDA flagged lack of clearance. The Class II medical device was distributed nationwide in the United States. The hazard is lack of FDA clearance. Consumers should stop use immediately and follow manufacturer guidance.
MicroPort Orthopedics recalled 91 units of the HIPTURN Fem Head Trial 36mm Reusable device on December 19, 2025. The recall follows the lack of FDA premarket authorization for distribution in the United States. The affected devices were distributed across multiple states and several countries, posing a potential health risk to patients and healthcare providers.
Feel The Beard recalled its minoxidil beard growth serum on December 18, 2025, due to a serious poisoning risk. The packaging fails to meet child-resistant requirements, which could lead to severe injury or death if ingested by young children. Consumers must stop using the product immediately and contact the company for further instructions.
Wilson-Cook Medical recalled 153 units of its Bipolar Sphincterotomes on December 18, 2025. A void in the device's material may cause an inappropriate electrical current during use. The recall affects specific models distributed in California, Colorado, Indiana, and North Carolina.
Waterfront BISTRO brand Frozen Raw Shrimp was recalled on December 18, 2025, due to possible contamination with Cesium-137. Approximately 1,800 cases of the product are affected. Consumers should not consume the shrimp and seek a refund or replacement.
Vascutek recalled 37,430 Gelsoft Plus and Gelweave vascular prostheses distributed nationwide in the United States after discovering the devices were labeled with an extra month of shelf life. The expiry date was calculated from packaging rather than gel impregnation. Healthcare providers and patients should stop using the devices immediately and follow recall instructions.
JOKOSIS recalled its HC0262 Adult Portable Bed Rails on December 18, 2025, due to serious entrapment hazards. Consumers face risks of asphyxiation if they become trapped between the bed rail and mattress. The bed rails lack the required safety labels and violate mandatory standards.
Pedego Electric Bikes recalled its Fat Tire Trikes on December 18, 2025, due to fall and laceration hazards. The trikes can develop hairline fractures near the welds, leading to potential accidents. Consumers should stop using the product and contact Pedego for a free repair.
Aju Pharm Co. recalled 200 units of the Genesis Push-In Suture Anchor on December 17, 2025. Users reported serious device failures including anchor breakage and suture breakage. Consumers and healthcare providers must stop using the device immediately.
Aju Pharm Co. recalled 1,163 units of Genesis Knotless Anchor on December 17, 2025, after reports of device failures. Issues include anchor breakage and suture breakage. Patients and healthcare providers must stop using the device immediately.