Browse through 2,317 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Diasol recalled 186,000 containers of its liquid concentrate for bicarbonate dialysis on November 5, 2025. The company cannot assure the safety and efficacy of the product. Patients and healthcare providers should stop using it immediately and follow recall instructions.
Diasol recalled 2,200 gallons of its 100425-10-DEX100 liquid concentrate for bicarbonate dialysis on November 5, 2025. The company cannot assure the safety and efficacy of the product. Patients and healthcare providers should stop using it immediately.
Diasol recalled 7,200 gallons of its 100125-10-DEX100 liquid concentrate on November 5, 2025. The recall affects dialysis patients in multiple states due to unassured safety and efficacy. Patients and healthcare providers must stop using this product immediately.
Diasol recalled 4,400 gallons of its 100230-10-DEX100 dialysis acid concentrate on November 5, 2025. The company cannot assure the safety and efficacy of this product. Healthcare providers and patients must stop using the concentrate immediately.
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.
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.
Datascope recalled 11,470 Intra-Aortic Balloon Pump systems on November 4, 2025. The recall addresses a revision in the Preventative Maintenance schedule as outlined in the Service Manual. Healthcare providers and patients must stop using these devices immediately.
Africa Imports recalled Organic Moringa Leaf Powder on November 4, 2025, after it tested positive for Salmonella. The recall affects 31 units of M-P697KG sold in several states, including Texas and New York. Consumers should not consume the product and seek a refund immediately.
Datascope recalled 47 units of its Cardiosave Rescue Intra-Aortic Balloon Pump on November 4, 2025. The recall addresses a revised Preventative Maintenance schedule in the device's instructions for use. This issue poses a high risk to patient safety and requires immediate attention from healthcare providers.
Mangalm LLC recalled Tops Mixed Fruit Jam on November 4, 2025, due to the presence of an unapproved color, carmoisine. Consumers should not consume the product and should seek a refund or replacement. The affected jam has a UPC of 8 904288 626025 and a best before date of June 10, 2026.
Tops Strawberry Jam was recalled on November 4, 2025, due to the presence of an unapproved color additive, carmoisine. Consumers should not consume the product, which was distributed in California. The jam, manufactured by G.D. Foods Mfg. in India, has a best-before date of June 10, 2026.
Tai Phat Wholesalers recalled seedless red dates on November 4, 2025, due to undeclared sulfites. The recall affects 10 cases containing 50 packages of 12 oz each. Consumers should not consume the product and seek refunds.
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.
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 one unit of its Organic Acids Profile Test Large on November 3, 2025. The recall occurred due to distribution without necessary premarket approval. Patients and healthcare providers should stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled one medical device on November 3, 2025, due to distribution without premarket approval. The recall affects the entire lot and requires immediate cessation of use. Patients and healthcare providers must follow the manufacturer’s instructions for safe disposal or return of the product.
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.
GET TESTED INTERNATIONAL AB recalled one unit of its Drug Test Small on November 3, 2025. The recall occurred due to distribution without premarket approval or clearance. The FDA classified this recall as Class II, indicating a high risk to patients and healthcare providers.
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.
GET TESTED INTERNATIONAL AB recalled 528 syphilis test units on November 3, 2025. The recall follows the distribution of the test without necessary premarket approval. Patients and healthcare providers should stop using the device immediately.