527 recalls tagged with “adult product”.
Cipla USA, Inc. recalled 63,504 bottles of Cinacalcet Hydrochloride Tablets on November 14, 2025. The recall results from a nitrosamine impurity, N-nitroso-cinacalcet, exceeding acceptable daily intake limits. Consumers should stop using the tablets immediately and contact healthcare providers for guidance.
Face Rock Creamery recalled 16 units of Vampire Slayer Garlic Cheddar cheese on November 14, 2025. The recall follows the discovery of Listeria monocytogenes in the processing area. Consumers should not consume the product and seek a refund or replacement.
Cipla USA, Inc. recalled 15,744 bottles of Cinacalcet Hydrochloride Tablets on November 14, 2025. The recall follows the discovery of a nitrosamine impurity exceeding acceptable daily intake limits. Consumers should stop using the product immediately and consult healthcare providers.
Genepro Protein, Inc. recalled 250 bags of Genepro Whey 4th Generation Plasma Treated Protein on November 12, 2025. The product is mislabeled and fails to declare milk as an allergen, posing a serious risk to consumers with dairy allergies. The affected product has a 'Best By' date of February 13, 2027.
Walgreens recalled 41,328 bottles of Saline Nasal Spray on November 12, 2025. The recall follows a discovery of microbial contamination by pseudomonas lactis. Consumers should stop using the product immediately and seek guidance from healthcare providers.
Pacific Seafood recalled 15,498 pounds of Raw Blackened Shrimp on November 8, 2025. The shrimp may contain undeclared sulfites, posing a health risk to sensitive individuals. The affected products were distributed in Alabama, Florida, and Massachusetts.
Anthony's Barbecue & Dip-It Sauce is recalled due to an undeclared fish allergen. The recall affects 192 glass bottles with UPC 6 89076 62272 1. Consumers should not consume the sauce and contact the company for a refund.
Actavis Laboratories recalled 15,944 cartons of Testosterone Gel on November 7, 2025. The recall follows a defect in the side-seal of the containers, which may allow product leakage. Consumers must stop using the product immediately and contact their healthcare providers for guidance.
Lezyne USA recalled bicycle floor pumps on November 6, 2025, due to a serious injury risk. The recall affects the Pressure Over Drive and Digital Pressure Over Drive models. The pumps can eject forcefully from the base when pressurized, posing a risk to users and bystanders.
C.R. Bard recalled 116 units of its InLay Optima Ureteral Stent Kit on November 6, 2025. A labeling discrepancy may cause the actual size of the stent to differ from what is indicated on the label. The recall affects distribution across the U.S. and several countries worldwide.
Neaude recalled adult portable bed rails on November 6, 2025, due to serious injury and death risks. The model BR0221SL001 poses an entrapment hazard that can lead to asphyxiation. Consumers should stop using the product immediately and seek a refund.
Hyundai recalled certain 2025 IONIQ 5 vehicles on November 4, 2025, due to braking software issues. The integrated electronic brake and vehicle control unit may cause reduced braking performance and unintended acceleration. Owners must refrain from using left-foot braking or N e-shift features until repairs are completed.
Ford recalled certain 2025 Explorer vehicles due to powertrain control module issues. The module may reset while driving, risking vehicle rollaway or engine stall. Notification letters were mailed to owners on June 6, 2025.
GET TESTED INTERNATIONAL AB recalled 5 units of its Food Intolerance Test Small on November 3, 2025. The recall follows the distribution of the device without necessary premarket approval. Healthcare providers and patients must cease use immediately and follow the manufacturer's instructions.
GET TESTED INTERNATIONAL AB recalled 94 units of its Parasite Test on November 3, 2025. The recall stems from distribution without premarket approval or clearance. Patients should stop using the device immediately and follow provided instructions.
GET TESTED INTERNATIONAL AB recalled 33 units of its sperm test on November 3, 2025. The recall stems from distribution without premarket approval or clearance. Patients and healthcare providers must stop using the device immediately.
Orthofix U.S. recalled 61,977 units of the CONSTRUX Mini PTC Spacer System on November 3, 2025. The recall impacts various model numbers due to inconsistent labeling claims. Consumers should stop using the product immediately and follow manufacturer instructions for a refund.
Dreyer's Grand Ice Cream recalled 3,410 cases of Haagen-Dazs mini chocolate dark chocolate ice cream bars on November 3, 2025. The recall occurred due to undeclared wheat, which poses a serious health risk to individuals with wheat allergies. The affected products were distributed in California, Kentucky, Ohio, and Wisconsin.
GET TESTED INTERNATIONAL AB recalled 184 units of Menopause (FSH) 2 Tests on November 3, 2025. This recall occurred due to distribution without premarket approval or clearance. Healthcare providers and patients must stop using the tests immediately and follow recall instructions.
GET TESTED INTERNATIONAL AB recalled 2,043 units of its 8 in 1 STI Test Kit on November 3, 2025. The recall resulted from distribution without premarket approval. Patients and healthcare providers must stop using the device immediately.