Manufacturer
101 recalls in our database name Philips Ultrasound, Inc as the manufacturing or recalling firm.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
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.
FDA is recalling Philips C9-3v Transducer Probes to provide clarification and labeling regarding the useful life of the devices. Approximately 171,322 units were distributed throughout the United States.
Philips is recalling C10-4ec ultrasound transducer probes nationwide to provide clarification and labeling regarding the useful life of these devices. 171,322 units are affected.
Philips Ultrasound is clarifying labeling on 171,322 VL13-5 transducer probes distributed nationwide to better define the useful life of the equipment.
Philips is clarifying labeling on its 3D9-3v ultrasound transducer probes to define their useful life. The recall affects 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 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 Ultrasound recalls 171,322 L15-7io transducer probes nationwide to provide labeling clarification defining the useful life of ultrasound transducers.
Philips Ultrasound is clarifying labeling on 171,322 3D6-2 Transducer Probes to better define the useful life of these ultrasound devices. This Class III recall affects units distributed nationwide.
Philips is clarifying labeling on 171,322 X11-4t ultrasound transducer probes to define their useful life in clinical use. This Class III recall affects devices distributed nationwide in the US.
Philips is clarifying labeling on 171,322 S8-3 Transducer Probe units to better define the useful life of ultrasound transducers in clinical use.
Philips Ultrasound is providing clarification on labeling for the C10-3v Transducer Probe to define the useful life of the product in clinical use.
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 approximately 171,322 S8-3t Transducer Probes distributed nationwide in the US to provide clarification and labeling regarding the device's useful life.
Philips Ultrasound is recalling the C10-3v Transducer Probe to provide clarification and labeling that defines the product's useful life. The recall affects 171,322 units distributed nationwide.
Philips is recalling 171,322 S4-1 Ultrasound Transducer Probes to provide clarification and labeling regarding the devices' useful life in clinical use. This FDA Class III recall affects healthcare facilities nationwide.
Philips is recalling 171,322 V6-2 Transducer Probes nationwide to provide labeling clarification defining their useful life. No injuries have been reported.
Philips is recalling 171,322 units of the L12-5 50 Transducer Probe to provide clarification and labeling regarding the product's useful life. This labeling correction affects ultrasound transducers distributed nationwide.
Philips Ultrasound is recalling the C9-4 Transducer Probe (171,322 units) nationwide to provide labeling clarification about the device's useful life.
Philips is recalling approximately 171,322 D2TCD Transducer Probes nationwide to provide clarification and labeling regarding the useful life of ultrasound transducers.
Philips Ultrasound is recalling 171,322 X8-2t Transducer Probe units distributed nationwide to provide labeling clarification regarding the devices' defined useful life.
Philips Ultrasound is recalling 171,322 L8-4 Transducer Probes to provide clarification and labeling defining the useful life of the ultrasound transducers.
Philips Ultrasound recalls 171,322 C9-2 Transducer Probe units to provide clarification and labeling defining the useful life of these medical ultrasound transducers. No illnesses or injuries have been reported.