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.
2,247 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
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.
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.
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 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.
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 recalled over 3.5 million bags of frozen okra on September 5, 2025, after tests revealed contamination with Salmonella. Consumers should not eat the product and seek refunds or replacements. The recall affects multiple lot numbers sold 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.
Par Pharmaceutical recalled 1,041 cartons of Everolimus tablets on September 5, 2025. The recall stems from failed impurities and degradation specifications. Consumers should stop using the product immediately.
Spacelabs Healthcare recalled 820 DVI display cables on September 5, 2025. The cables may interfere with other medical devices due to inadequate shielding. Patients and healthcare providers should stop using these cables immediately.
Spacelabs Healthcare recalled 8,179 DVI display cables on September 5, 2025, due to electromagnetic interference issues. The cables can interfere with sensitive medical devices, posing serious safety risks. Patients and healthcare providers 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.