2,756 recalls tagged with “immediate action”.
Iantrek recalled 1,262 CycloPen CP-300 Cyclodialysis System units distributed nationwide to medical facilities. The recall stems from a potential compromise to sterile packaging integrity. Hospitals and clinics should stop using the device immediately and follow Iantrek’s recall instructions via email.
Sandoz Inc. recalled 263 vials of Cyclophosphamide injection distributed nationwide in the United States. The recall cites cGMP deviations due to a temperature excursion during transportation. Healthcare providers and patients should stop using the product and contact Sandoz for guidance.
Spacelabs Healthcare is recalling 16,898 DVI display cables worldwide, including the United States. The cables are used as external display connectors for certain monitors. The recall follows a risk that inadequately shielded cables may cause electromagnetic interference with other medical devices. Stop using the affected cables immediately and await manufacturer instructions.
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.
Spacelabs Healthcare recalls 8,179 DVI display cables worldwide after EMI interference could affect medical monitors. The cables connect 6-foot DVI-I to DVI-I devices used with the 91390 and 91393 monitors. Healthcare providers should stop using affected cables and follow recall instructions.
Apotex Inc. recalls Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution sold nationwide in the US. The recall cites lack of assurance of sterility due to improper bottle sealing. 151,034 bottles affected. Consumers should stop using the product immediately.
GE Medical Systems recalled 7,302 AW Server models worldwide, including 1,381 units in the U.S., after identifying a security vulnerability that could expose patient data. The defect could allow a malicious actor to compromise confidentiality, integrity and availability of information. Healthcare providers should stop using the devices immediately and follow manufacturer instructions for recall.
GE Healthcare recalled 173 CSCS MAS800 Central Station desktops distributed worldwide to hospitals after identifying a software fault that can trigger a reboot cycle. The reboot can result in a loss of central patient monitoring. Hospitals should stop using the devices and follow the manufacturer’s recall instructions.
Spacelabs Healthcare has recalled 820 DVI display cables worldwide due to shielding issues that may cause electromagnetic interference with other medical devices. The cables connect monitors used in patient care. Hospitals should stop using the affected cables and follow manufacturer recall instructions. The recall was issued by letter and is active as of 2025.
Endo USA, Inc. recalled 1,041 cartons of Everolimus 5mg tablets nationwide in the United States due to an impurity IP-C out of specification. The impurity IP-C is out of specification in the drug product. Patients and healthcare providers should stop using this product immediately and contact Endo USA or their healthcare provider for guidance.
GE Healthcare recalled 2,306 CSCS V3 MAS800 Central Station desktops worldwide after identifying a software fault that can trigger a continuous reboot cycle. The issue can result in a loss of central monitoring for connected patients. Hospitals should stop using the affected devices and follow the recall instructions from GE HealthCare and Wipro GE Healthcare Private Ltd.
Philips Ultrasound, Inc. recalled 41 S4-1 Ultrasound Transducers distributed nationwide in the United States. The recall is to provide clarification and labeling to define the useful life of ultrasound transducers in the field. Healthcare providers should stop using these devices immediately and follow the recall instructions from Philips or their facility.
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 17 X3-1 ultrasound transducers nationwide in the United States. The recall is to provide clarification and labeling to define the useful life of transducers in the field. Healthcare providers and patients should stop using the affected devices immediately and await further manufacturer instructions.
Philips Ultrasound recalled 1 unit of the S5-2 Ultrasound Transducer sold nationwide through healthcare distributors. The recall clarifies labeling to define the useful life of the transducer in the field. Healthcare providers should stop using the device and contact Philips Ultrasound for instructions.
Philips Ultrasound recalled 11 Mini Multi TEE ultrasound transducers distributed nationwide in the United States after a labeling clarification related to useful life. The recall centers on providing clarification and labeling to define the useful life of transducers in the field. Healthcare providers should stop using the device and follow recall instructions from Philips Ultrasound, Inc or their
Philips Ultrasound recalled 75 OMNI III TEE Ultrasound Transducers distributed nationwide in the United States. The recall concerns labeling to define the useful life of these transducers in the field. Healthcare facilities should stop using the devices immediately and follow the recall instructions from Philips Ultrasound, Inc.
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.
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.
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.