527 recalls tagged with “adult product”.
GET TESTED INTERNATIONAL AB recalled six units of its Food Intolerance Test on November 3, 2025. The recall stems from the distribution of the product without premarket approval or clearance. Healthcare providers and patients must stop using the device immediately.
Orthofix U.S. LLC recalled 13,317 PTC Spacer Systems on November 3, 2025, due to inconsistent labeling claims. The recall affects multiple model numbers sold worldwide, including in the U.S. The company advises immediate cessation of use and communication with healthcare providers.
Nissan recalled certain 2025 Sentra vehicles on November 3, 2025. The driver's seat frame may not be fully secured, increasing crash injury risk. Owners received notification letters starting May 1, 2025.
Stryker Corporation recalled 39,148 BrainPath devices on October 31, 2025, due to a latex allergy risk. The tape used to secure components contains latex, despite being labeled latex-free. This recall affects devices distributed worldwide, including the U.S. and multiple countries.
Stryker recalled 39,148 NICO Myriad Handpieces on October 31, 2025, due to a latex hazard. The packaging tape contains latex despite products being labeled latex-free. This poses a significant allergy risk to patients and healthcare providers.
Trifecta Pharmaceuticals recalled 33,000 containers of Globe Zinc Oxide Ointment on October 31, 2025, due to cGMP deviations. Consumers should stop using the product immediately to avoid potential risks. Healthcare providers are advised to contact the company for further guidance.
Aizu Olympus recalled 6,578 OER-Elite medical devices following safety concerns. The recall, announced on October 31, 2025, urges patients and healthcare providers to stop using the device immediately. Repairs should only be conducted by trained personnel to ensure safety.
Nivagen Zinc Oxide Ointment 20% skin protectant, manufactured in India for Nivagen Pharmaceuticals and distributed nationwide in the USA, is recalled. The recall covers 912 containers. The defect cited is cGMP deviations. Consumers and healthcare providers should stop using the product and follow guidance from Blossom Pharmaceuticals or a healthcare professional.
Polaris Industries recalled certain 2025-2026 Ranger XP 1000 NorthStar and Ranger Crew XP 1000 ROVs due to a fire hazard. The recall affects vehicles sold between March 2025 and August 2025. Polaris urges consumers to stop using the recalled vehicles immediately.
Knog recalled the Blinder 900 and Blinder 1300 Front Bicycle Lights on October 30, 2025, due to fire hazards. The lithium-ion batteries can overheat and ignite, presenting a serious risk to users.
Werner Paddles recalled Stealth and Covert kayak paddles on October 30, 2025. The paddles can break during use, creating a drowning hazard. Consumers should stop using the paddles and seek a refund immediately.
Avenco and Novilla recalled mattresses on October 30, 2025, due to a fire hazard. The mattresses violate mandatory flammability standards, posing a risk of serious injury or death. Consumers should stop using the products immediately and contact the manufacturer for a remedy.
B Braun Medical recalled 40,992 IV administration sets on October 29, 2025. The recall addresses a potential for backflow of medication from secondary IV containers into primary containers. This issue may lead to serious health risks for patients.
B Braun Medical recalled 11,832 IV administration sets on October 29, 2025. The recall affects models catalog numbers 490315, 490331, and 490376. The device poses a risk of medication backflow and occlusion during use.
B Braun Medical recalled 18,072 IV administration sets on October 29, 2025. The recall affects the Outlook set utilized with Infusomat Space and Outlook Pumps. The sets pose a high risk of medication backflow and priming issues.
Avion Pharmaceuticals recalled 804 bottles of Prenate Chewable vitamins on October 29, 2025, due to undeclared soy. The recall affects consumers in 15 states, including California and Texas. The product also contains a labeling error regarding the amount of boron.
B Braun Medical recalled 100 IV administration sets on October 29, 2025, due to a backflow risk. The recall affects gravity IV and pump administration sets used with several infusion pumps. The potential for medication backflow poses a serious health risk to patients.
B Braun Medical recalled 43,900 IV administration sets on October 29, 2025. The recall affects devices used with Infusomat Space, Outlook, and Vista Basic Pumps. Users must stop using these devices immediately due to a potential medication backflow hazard.
B Braun Medical recalled 2,544 IV Administration Sets on October 29, 2025. The recall follows reports of potential backflow of medication from secondary IV containers into primary IV containers. Healthcare providers and patients should stop using the devices immediately.
B Braun Medical recalled 5,952 IV administration sets on October 29, 2025. The recall stems from a risk of medication backflow from secondary IV containers. This poses a serious health risk for patients receiving treatment.