2,715 recalls tagged with “immediate action”.
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.
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.
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.
Philips recalled 17 units of the 3D6-2 Ultrasound Transducer distributed nationwide to healthcare facilities in the United States. The recall seeks to clarify labeling defining the transducer’s useful life. Clinicians and facilities should stop using the device immediately and follow Philips recall instructions.
Deep-brand PREMIUM Select Fansi Cut French Beans have been recalled after testing positive for Salmonella. The recall affects approximately 3,509,532 bags distributed across the United States. Consumers should not consume the product and seek a refund 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.
CHETAK NEW YORK recalled 3,509,532 bags of its Premium Select Suran on September 5, 2025. The product tested positive for Salmonella, posing a serious health risk to consumers. Customers should stop using the product immediately and seek a refund or replacement.
Chetak New York LLC recalled over 3.5 million bags of frozen Arvi on September 5, 2025, after testing positive for Salmonella. Consumers should not consume the product due to serious health risks. The recall affects multiple lot numbers sold across the United States.
Chetak New York recalled over 3.5 million bags of Surti Undhiu Mix on September 5, 2025, after the product tested positive for Salmonella. The recall affects multiple lot numbers of the 12 oz. frozen vegetable mix distributed across the United States.
Philips Ultrasound recalled 5 X7-2 ultrasound transducers distributed nationwide to healthcare providers. The recall is to provide clarification and labeling to define the useful life of ultrasound transducers in the field. Healthcare facilities should stop using the recalled devices and follow Philips Ultrasound, Inc instructions or contact their provider for guidance.
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.
Philips Ultrasound recalled 2 units of the Philips OMNI II TEE Ultrasound Transducer sold nationwide through multiple retailers. The recall seeks labeling clarification to define the transducer's useful life. Healthcare facilities should stop using the devices and follow Philips recall instructions.
Philips Ultrasound recalled 1 unit of the C9-4 Ultrasound Transducer, Model No. 989605365021, distributed nationwide in the United States. The recall focuses on clarifying and labeling the device’s useful life. Healthcare providers and patients should stop using the device immediately and follow Philips’ instructions for replacement or further steps.
CHETAK NEW YORK recalled 3,509,532 bags of PREMIUM Select Green Garlic on September 5, 2025, after testing positive for Salmonella. The recall affects products distributed throughout the United States. Consumers should not eat the product and should seek a refund or replacement.
Chetak New York recalled over 3.5 million bags of frozen green chili on September 5, 2025. The product tested positive for Salmonella, a serious foodborne pathogen. Consumers should not consume the product and seek refunds immediately.
CHETAK NEW YORK recalled over 3.5 million bags of Dum Aloo on September 5, 2025, after testing positive for Salmonella. The recall affects products distributed throughout the United States. Consumers should not eat the product and seek a refund or replacement.
Two Philips Ultrasound L17-5 transducers distributed nationwide to hospitals are recalled. The recall targets labeling that defines the devices' useful life. Stop using the transducers and follow Philips Ultrasound's instructions. Hospitals should contact Philips Ultrasound for guidance.