Browse through 2,313 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Whole Foods Market recalled Blueberry Almond Granola on September 9, 2025. The product contains undeclared allergens including wheat, sesame, and cashew. Six units, packaged in one-pound containers, were sold at one store in Philadelphia, PA.
Lotsa Pasta International Food Shop recalled 54 bottles of Fresh Basil Infused Olive Oil on September 9, 2025. The product may be contaminated with Clostridium botulinum due to improper manufacturing processes. Consumers should not consume the product and seek a refund or replacement.
Hale recalled 54 bottles of Roasted Garlic Infused Olive Oil on September 9, 2025. The product may be contaminated with Clostridium botulinum and was manufactured without an approved process. Consumers should stop using the product immediately and seek a refund or replacement.
BioPro recalled 147 femoral heads on September 9, 2025, due to a packaging defect. The defect threatens the sterility of the device, which could lead to infection if implanted. Healthcare providers and patients must stop using these devices immediately.
BioPro recalled 147 units of Endo Heads on September 9, 2025. A packaging issue may compromise the sterile barrier, leading to infection risk. Healthcare providers and patients should stop using the devices immediately.
BioPro recalled 147 bipolar heads on September 9, 2025, due to a potential packaging issue. The defect may compromise the sterile barrier, increasing infection risks if implanted. Healthcare providers and patients should stop using these devices immediately.
Draeger recalled 223 Atlan A350XL anesthesia workstations on September 9, 2025. The devices may fail during mechanical ventilation, posing serious health risks. The recall affects states across the U.S. and several countries worldwide.
BioPro recalled 147 femoral head components on September 9, 2025. A packaging defect may compromise sterility, increasing infection risk. The recall affects models distributed in Texas and Michigan.
Eureka recalled 32 cases of cinnamon on September 9, 2025, due to elevated lead levels. Consumers should not consume the product and seek refunds. The recall affects retail and wholesale customers in California and Michigan.
NOXBOX recalled 1,667 Nitric Oxide Delivery Systems on September 9, 2025. The recall follows reports of internal faults caused by rapid button selections. The company advises patients and healthcare providers to stop using the device immediately.
Draeger recalled 530 Atlan A350 anesthesia workstations due to potential ventilation failures. The recall occurred on September 9, 2025, after reports of critical device malfunctions during use. Patients and healthcare providers must stop using the device immediately.
MedicalCommunications GmbH recalled 474 units of HEYEX PACS software on September 9, 2025. The software may inaccurately report measured values, posing risks to patient care. Users should stop using the software immediately and follow recall instructions.
NOXBOX recalled 1,667 Nitric Oxide Delivery Systems on September 9, 2025. The recall stems from dangerous dose fluctuations that could occur under specific device settings. Healthcare providers and patients should stop using the device immediately.
Lee K of NY Inc. recalled 43 units of Aged Kimchi Mackerel on September 8, 2025. The product contains undeclared milk and shrimp, posing a serious allergy risk. Consumers in New York and New Jersey should stop using the product immediately.
Iantrek recalled 1,262 units of the Cyclopen Microinterventional Cyclodialysis System on September 6, 2025. The recall stems from a risk of compromised sterile packaging that could affect patient safety. Health care providers and patients must stop using the device immediately and follow manufacturer instructions.
Iantrek recalled 198 C-Rex UNO Microinterventional Goniotomy Instruments on September 6, 2025, due to compromised sterile packaging. The recall affects the model CRX-120 distributed in multiple U.S. states. Healthcare providers and patients must stop using these instruments immediately.
Sandoz Inc. recalled 263 vials of Cyclophosphamide Injection on September 5, 2025. The recall follows cGMP deviations related to temperature excursions during transportation. Healthcare providers and consumers must stop using the product immediately.
Chetak New York LLC recalled over 3.5 million bags of frozen baby bhindi on September 5, 2025, due to potential Salmonella contamination. The recall affects the Deep-brand Premium Select Baby Bhindi, weighing 12 oz. Consumers should not consume this product and seek refunds immediately.
Deep-brand recalled 3.5 million bags of PREMIUM Select Sweet Corn on September 5, 2025, due to Salmonella contamination. The affected product weighs 2 pounds and was distributed across the United States. Consumers should not consume this product and should seek a refund.
Chetak New York recalled over 3.5 million bags of frozen Tuvar Lilva on September 5, 2025. The product tested positive for Salmonella, posing a significant health risk. Consumers should not consume this product and seek a refund or replacement immediately.