Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Minimum severity
Philips Ultrasound is recalling 171,322 X5-1c Transducer Probes distributed nationwide to provide clarification and labeling that defines the useful life of the devices in the field.
Philips Ultrasound is recalling 171,322 units of the D5cwc Transducer Probe nationwide to provide labeling clarification and define the product's useful life.
Philips is clarifying labeling on S5-2 ultrasound transducer probes to better define how long they can be safely used. The manufacturer is providing guidance to healthcare facilities on proper device replacement schedules.
Philips is recalling 171,322 L11-3 ultrasound transducer probes to provide clarification and labelling defining the devices' useful life. Units were distributed nationwide.
Philips is recalling the S4-1 Lumify Transducer Probe to provide clarification and labeling that defines the useful life of ultrasound transducers. The recall affects 171,322 units distributed nationwide.
HOMEDICS Air Compression Leg Massager (Model SR-160HJ) is being recalled due to a regulatory documentation error and misleading color packaging claim. Approximately 3,705 units have been distributed in the United States and Canada.
Orascoptic Surgical Acuity is recalling Dragonfly nose pad kits because they contain nickel, which may cause allergic reactions in sensitive users.
Philips Ultrasound is recalling 171,322 C8-5 Transducer Probe units nationwide to provide clarification and labeling regarding the devices' useful life.
Philips Ultrasound is clarifying labeling for 171,322 Mini Multi TEE transducer probes to better define the devices' useful life in clinical use.
Philips is recalling 171,322 mC7-2 Transducer Probes distributed nationwide to clarify labeling defining the useful life of ultrasound transducers. No injuries or illnesses have been reported.
Philips Ultrasound is clarifying labeling on 171,322 units of 7.5MHz Endo Transducer Probes to properly define device useful life. Devices were distributed nationwide.
BD Pyxis automated medication dispensing systems are recalled because antivirus software was not consistently installed during the implementation process, affecting 8,353 devices worldwide.
The THOR NovoTHOR Gen 3.0 Reg PRX therapeutic heating device may have a faulty welded nut that can shear off. This causes the gas strut to detach, making the canopy difficult to lift and potentially affecting device use.
Philips Ultrasound is recalling 171,322 L12-5 Transducer Probes to clarify labeling that defines useful life. The Class III recall affects devices distributed nationwide in the US.
Philips is recalling approximately 171,322 S7-2t Transducer Probe units to provide labeling clarification and define the product's useful life.
Philips Ultrasound is providing clarification and updated labeling to define the useful life of C8-4v transducer probes. This is a labeling update affecting approximately 171,322 units distributed nationwide.
Philips is recalling 171,322 L18-5 Transducer Probes nationwide to provide clarification and labeling defining the useful life of ultrasound transducers.
Philips Ultrasound is issuing a labeling clarification for approximately 171,322 X7-2t transducer probes to define their useful life for clinical use.
Philips Ultrasound is recalling 171,322 L12-4 Transducer Probes distributed nationwide to provide clarification and updated labeling regarding the useful life of the ultrasound transducers.
Philips Ultrasound is issuing labeling clarification for approximately 171,322 X6-1 Transducer Probes distributed nationwide to define the useful life of these devices.
Philips Ultrasound recalls 171,322 eL18-4 Transducer Probes to clarify labeling regarding the transducers' useful life. The FDA Class III recall is intended to ensure proper use within the transducers' functional parameters.
Philips is clarifying labeling on 171,322 ultrasound transducer probes nationwide to define the useful life of the devices. No injuries have been reported.
Philips is recalling approximately 171,322 L12-4 Lumify Transducer Probes distributed nationwide to provide clarification and updated labeling defining the useful life of ultrasound transducers.
Philips issues labeling clarification for the C5-2 Lumify Transducer Probe to define useful life of ultrasound transducers. The recall affects approximately 171,322 units distributed nationwide in the US.
Philips Ultrasound is recalling 171,322 S9-2 Transducer Probe units distributed nationwide to provide clarification and labeling regarding the devices' useful life.