989 recalls tagged with “adult product”.
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.
GET TESTED INTERNATIONAL AB recalled 12 Peptic Ulcer Tests for H. pylori sold nationwide through multiple retailers. The tests were distributed without FDA premarket approval or clearance. Health professionals and patients should stop using the tests immediately and await recall instructions.
GET TESTED INTERNATIONAL AB distributed 1 unit nationwide in the United States. The device lacked premarket approval or clearance. Stop using the product immediately and contact GET TESTED INTERNATIONAL AB for instructions.
GET TESTED INTERNATIONAL AB recalled 5 chlamydia test devices distributed nationwide in the United States after regulators found distribution without FDA premarket approval or clearance. The devices lack required premarket authorization. Patients and healthcare providers should stop using the device immediately and follow the manufacturer's recall instructions.
GET TESTED INTERNATIONAL AB's Lyme Test devices were distributed nationwide in the United States to healthcare providers. Regulators found the devices were distributed without FDA premarket approval or clearance. Healthcare providers and patients should stop using the device immediately and follow recall instructions.
Get Tested International AB recalled 1,210 units of its 3 in 1 STI Test distributed nationwide in the U.S. The product was distributed without FDA premarket approval or clearance. Patients and healthcare providers should stop using the device immediately and follow the recall instructions.,
GET TESTED INTERNATIONAL AB recalled 3 units of its Food Allergy Panel Test (IgE) distributed nationwide in the United States after distribution without premarket approval was identified. The recall pertains to a regulatory lapse rather than an announced safety defect. Consumers should stop using the device immediately and follow manufacturer instructions.
Philips North America recalled 1,913,441 IntelliVue MX100 patient monitors due to potential alarm failure. The recall is active as of December 2025. The manufacturer warns patients and healthcare providers to stop using affected devices and follow recall instructions. Contact Philips North America LLC for guidance.
Stryker recalled 39,148 NICO BrainPath BrainPath Shephard's Hook devices distributed worldwide through multiple healthcare providers. latex-containing tape in packaging is the defect, despite latex-free labeling. Stop using the device now and follow recall instructions from Stryker or your healthcare provider.
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.
Philips North America LLC is recalling 1,913,441 IntelliVue MP5 patient monitors sold to hospitals worldwide. The devices may fail to alarm, delaying detection of patient distress. Hospitals and clinicians should stop using the monitors immediately and follow Philips recall instructions.
Blonde Beard's recalled 4,888 bottles of Dojo Asian Wing Sauce sold through multiple retailers in the United States and Canada after confirming undeclared soy on the label. The sauce is shelf-stable and packaged in 8-ounce glass bottles. Consumers should not consume the product and should contact Blonde Beard's for refund or replacement.
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.
Philips North America LLC recalled 1,913,441 IntelliVue MP40 patient monitors worldwide after reports the monitors did not alarm. The issue could prevent alerts to clinicians about patient deterioration. Stop using the device and follow the recall instructions from Philips or your healthcare provider immediately.
Avenco and Novilla mattresses marketed by PT Champion are recalled for a serious fire risk. The recall covers models in 6, 10, 12 and 14 inches of thickness across twin to king sizes. Consumers should stop using these mattresses immediately and contact PT Champion for a free fitted cover or repair options.
Olympus Corporation of the Americas recalled 7,803 HX-400U-30 single‑use ligating devices distributed nationwide in the United States. The ligation loop may fail to release or detach. Hospitals and clinics should stop using the device immediately and follow the recall instructions from Olympus or their healthcare providers.
Werner Paddles recalls Stealth and Covert kayak paddles after determining they can break during use, creating a drowning hazard. The paddles sold by retailers nationwide and online from October 2023 through August 2025 for $470 to $560. Consumers should stop using the recalled paddles immediately and contact Werner Paddles for a full refund or store credit.
Crate & Barrel recalled Ana Dining Chairs sold at Crate & Barrel stores and Crateandbarrel.com from January 2021 through January 23, 2025 for a fall hazard. The chair legs can break, posing a fall risk. Stop using the recalled chair and contact Crate & Barrel to obtain a free replacement chair and arrange a free pickup.
B. Braun Medical recalled 49,330,370 Infusomat IV sets worldwide after a potential backflow from secondary to primary IV containers and an inability to prime. The recall covers gravity IV sets and pump sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Stop using any affected sets immediately and contact B. Braun Medical for instructions on refunds or replacement
B Braun Medical recalled 24,624 Blood Administration Sets worldwide. The recall covers sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The risk involves backflow from secondary IV containers into primary containers and the inability to prime. Hospitals and clinics should stop using the devices immediately and follow recall instructions.