989 recalls tagged with “adult product”.
Baker’s Authority recalled 70 units of Graham Cracker Meal on August 12, 2025. The product ships to multiple states. Undeclared wheat and soy allergens are listed on the label. The recall urges consumers to avoid consumption and seek refunds or replacements.
Max Mobility LLC and Permobil recalled 25,389 MX2-3DC SpeedControl Dial units used with the SmartDrive MX2+ wheelchair power assist. A faulty electrical connection between the speed control dial and the wheelchair motor can cause loss of control. Users should stop using the device immediately and follow the manufacturer’s recall instructions for next steps.
Max Mobility LLC recalls Permobil Smart Drive MX2+ SpeedControl Dial MX2-3DCK affecting 15,834 units sold through multiple retailers. A faulty electrical connection between the speed control dial and the wheelchair motor can cause loss of control. Stop using the device immediately and follow recall instructions; contact Max Mobility LLC or your healthcare provider for instructions. This recall was
Viona Pharmaceuticals recalls Tavaborole Topical Solution 5% 10 mL bottles, distributed nationwide in the U.S. The effective recall date is August 12, 2025. The product is manufactured by Zydus Lifesciences Ltd. Discoloration was cited as the reason for the recall. Consumers should stop using the product and contact the distributor for guidance.
Applied Medical Technology recalled 1,780 NutraGlide ENFit nasal feeding tubes distributed in Massachusetts and Rhode Island. Distal tips on these devices may detach at lower than expected forces. Stop using immediately and follow the recall instructions.
Applied Medical Technology recalls NutraGlide ENFit Nasal Feeding Tubes distributed to facilities in Massachusetts and Rhode Island. The distal tips may detach at lower than expected forces. Hospitals and patients should stop using the devices and follow recall instructions.
Applied Medical Technology recalled 840 NutraGlide ENFit nasal feeding tubes distributed in the United States to Massachusetts and Rhode Island. The tubes have distal tips that may detach at lower than expected forces. Healthcare providers and patients should stop using the device immediately and follow the recall instructions.
Applied Medical Technology recalled 200 NutraGlide ENFit nasal feeding tubes distributed in Massachusetts and Rhode Island. The distal tips may detach at lower than expected forces. Stop using the device immediately and follow the manufacturer’s recall instructions.
Lannett Company, Inc. recalls 8,544 bottles of Lisdexamfetamine Dimesylate 40 mg capsules distributed nationwide. A labeling mix-up may have placed 30 mg and 40 mg strengths in mislabeled bottles. Healthcare providers and patients should stop use and contact the company for guidance.
Baxter Healthcare Corporation issued an urgent medical device recall for one lot of Continu-Flo intravascular solution sets, 14,400 units distributed nationwide in the United States. Customer reports indicate tubing separation. Health care providers and patients should stop using the device immediately and follow recall instructions.
Glenmark Pharmaceuticals Inc. USA recalls theophylline extended-release 400 mg tablets after dissolution test failures. The recall covers 22,656 bottles distributed nationwide in the United States. Consumers should stop using the product and contact Glenmark for guidance.
Breckenridge Pharmaceutical recalls duloxetine delayed-release capsules due to CGMP deviations raising N-nitroso-duloxetine impurity above interim limit. The bottles were distributed to Arizona, Indiana and New Jersey. Consumers should stop using the product and contact their healthcare provider for guidance.
SUNGAL Inc. recalls 29 cases of UDK Half Plum, 170 g containers distributed to California, Maryland, New York and Virginia. The product is adulterated with cyclamate. Consumers should not consume it and should email SUNGAL Inc. for refund or replacement information.
Medline Industries recalled 88 units of the Sterile Extremity Pack DYNJ45701B after finding that kits labeled as sterile had not undergone sterilization. The affected distribution covered Florida, Maryland, New Jersey and Tennessee. Hospitals and clinics should stop using the kit immediately and follow Medline's recall instructions.
Schiller, AG recalls 266 Argus PB-3000 vital sign monitors nationwide in the United States. The devices may display an error message during blood pressure measurements when the initial inflation pressure is set high. Authorities urge users to stop using the device and follow manufacturer instructions.
Glenmark Pharmaceuticals Inc. recalls 6,432 bottles of Carvedilol Tablets, USP, 12.5 mg, distributed nationwide in the United States. The recall concerns CGMP deviations and the presence of a nitrosamine impurity above the acceptable intake level. Consumers should stop taking the product and contact Glenmark for guidance.
Deale International recalls Altafit AF28 smartwatches sold by HSN after reports of overheating charging pads. The recall cites a risk of serious burn injury and fire. Consumers should stop charging the watch immediately and contact Deale International for a free replacement.
Fieldsheer Apparel Technologies is recalling heated socks MWMS07, MWWS07 and MWMS05. The recall covers socks sold with two lithium-ion battery packs and a charging cable. Consumers should stop using the product and contact Fieldsheer for a refund or replacement.
Glenmark Pharmaceuticals Inc. recalls 44,328 bottles of Carvedilol tablets, 3.125 mg, distributed nationwide in the USA. The impurity N-nitroso carvedilol I exceeds the Acceptable Intake Level. Consumers should stop using the product and contact Glenmark for guidance.
Monica Vinader recalls select 14k yellow gold mini heart bracelets, necklaces and stud earrings due to high cadmium levels. The recalled jewelry was manufactured in October and November 2024. Consumers should stop wearing the jewelry immediately and contact Monica Vinader for a replacement or refund.