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 recalls 171,322 D2cwc Transducer Probes nationwide to provide clarification labeling on device useful life. Facilities should review updated labeling for proper device management and replacement schedules.
Philips Ultrasound is recalling approximately 171,322 X7-2 Transducer Probes distributed nationwide to provide clarification and labeling regarding the useful life of these ultrasound devices.
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 issued a nationwide recall of 171,322 C6-2 Transducer Probes to provide clarification and labeling defining the useful life of these ultrasound transducers.
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.
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 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 Ultrasound recalls 171,322 L15-7io transducer probes nationwide to provide labeling clarification defining the useful life of ultrasound transducers.
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 is clarifying labeling on 171,322 ultrasound transducer probes nationwide to define the useful life of the devices. No injuries have been reported.
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 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 recalling approximately 171,322 units of C8-4v Transducer Probes distributed nationwide to provide clarification and labeling defining the useful life of these ultrasound transducers.
Philips is recalling 171,322 L18-5 Transducer Probes nationwide to provide clarification and labeling defining the useful life of ultrasound transducers.
Philips is recalling the c5-1 Transducer Probe to clarify labeling defining device useful life. The recall affects approximately 171,322 units distributed nationwide.
Philips Ultrasound is recalling 171,322 X8-2t Transducer Probe units distributed nationwide to provide labeling clarification regarding the devices' defined 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 issuing labeling clarification for approximately 171,322 X6-1 Transducer Probes distributed nationwide to define the useful life of these devices.
Recall issued to clarify and improve labeling defining the useful life of Philips L9-3 Transducer Probes. Manufacturer providing documentation clarification to healthcare providers 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 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 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 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 clarifying labeling on its 3D9-3v ultrasound transducer probes to define their useful life. The recall affects approximately 171,322 units distributed nationwide.
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.