These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
2,251 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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 PREMIUM Select Diced Green Mango on September 5, 2025. The product tested positive for Salmonella, posing a serious health risk to consumers. The recall affects products distributed across the United States.
GE Healthcare recalled 2,306 Carescape Central Station devices on September 5, 2025, due to a software issue. The problem can cause a continuous reboot cycle, risking loss of patient monitoring. The recall affects devices with software version V3.0.5 when connected in specific network conditions.
GE Healthcare recalled 173 units of the Carescape Central Station on September 5, 2025. The device may enter a continuous reboot cycle, risking loss of patient monitoring. This issue occurs when 118 to 120 stations connect to the network.
Chetak New York recalled 3.5 million bags of frozen garlic cloves on September 5, 2025, due to potential Salmonella contamination. The recall affects products sold across the United States. Consumers should not consume the product and seek a refund.
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 PREMIUM Select Tapioca on September 5, 2025. The product tested positive for Salmonella, posing serious health risks. Consumers should not consume this product and seek refunds immediately.
Chetak New York LLC recalled over 3.5 million bags of frozen mixed vegetables on September 5, 2025, due to Salmonella contamination. Consumers should not eat the product and should seek refunds or replacements. The recall affects products distributed across the United States.
Chetak New York recalled over 3.5 million bags of PREMIUM Select Peas and Carrots on September 5, 2025. The recall follows positive tests for Salmonella, a dangerous pathogen. Consumers should not consume the product and seek refunds immediately.