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 S7-3t transducer probes nationwide to provide labeling clarification regarding the useful life of ultrasound transducers.
Philips Ultrasound, Inc. is recalling 171,322 C9-4v Transducer Probes nationwide. The recall provides labeling clarification regarding the useful life of these diagnostic ultrasound probes.
Philips Ultrasound, Inc. is recalling 171,322 L12-3 Transducer Probes nationwide to provide clarification and labeling regarding the useful life of ultrasound transducers in field use.
Philips Ultrasound is recalling 171,322 units of the C9-3io Transducer Probe to provide clarification and labeling regarding the useful life of the devices. Units were distributed nationwide in the United States.
Philips is recalling approximately 171,322 S7-2t Transducer Probe units to provide labeling clarification and define the product's useful life.
Philips Ultrasound recalls approximately 5,230 V6-2 ultrasound transducers that were refurbished beyond their useful life. The devices are distributed nationwide and internationally across more than 50 countries.
Philips is recalling 5,230 VL13-5 ultrasound transducers refurbished beyond their useful life, risking device degradation and failure in clinical use.
Philips is recalling 5,230 S8-3t ultrasound transducers because they were refurbished beyond their useful life. The devices were distributed nationwide and internationally to 56 countries.
Philips is recalling 5,230 ultrasound transducers that were refurbished beyond their useful life. Devices may not perform as designed and should not be used.
Philips Ultrasound is recalling approximately 5,230 X8-2t ultrasound transducers that were refurbished beyond their useful life. The devices were distributed nationwide and internationally.
Philips is recalling 5,230 S7-3t ultrasound transducers that were refurbished beyond their useful life. Devices operated beyond their intended operational lifespan may not perform reliably.
Philips recalls 3D9-3v ultrasound transducers that were refurbished beyond their useful life, risking unreliable device performance. About 5,230 units were distributed nationwide and to 50+ countries.
Philips Ultrasound is recalling 5,230 S7-2 transducers that were refurbished beyond their useful life. The devices were distributed nationwide and internationally and may not function reliably.
Philips Ultrasound is recalling 5,230 eL18-4 ultrasound transducers that were refurbished beyond their intended useful life. The devices may not function reliably.
Philips is recalling 5,230 XL14-3 ultrasound transducers that were refurbished beyond their useful life. The FDA classified this as a Class II recall; no injuries have been reported.
Philips Ultrasound is recalling 5,230 C5-2 Transducers that were refurbished beyond their useful life. The devices may not function reliably and have been distributed nationwide and internationally.
Philips Ultrasound is recalling 5,230 X6-1 transducer units that were refurbished beyond their useful life. These devices may not perform reliably due to refurbishment beyond manufacturer specifications.
Philips Ultrasound is recalling 5,230 C5-1 ultrasound transducers that were refurbished beyond their useful life, risking device malfunction or degraded diagnostic performance. The devices were distributed nationally and to more than 50 countries.
Philips is recalling 5,230 X7-2t ultrasound transducers that were refurbished beyond their useful life. Improperly refurbished devices may not perform as intended for diagnostic applications.
Philips Ultrasound is recalling approximately 5,230 L9-3 transducer units that were refurbished beyond their useful life, potentially affecting device reliability and performance.
Philips Ultrasound, Inc. is recalling 5,230 L8-4 ultrasound transducers that were refurbished beyond their useful life. The devices may not maintain proper performance specifications.
Philips is recalling 5,230 L12-4 ultrasound transducers that were refurbished beyond their design lifespan. Devices beyond useful life may experience performance degradation or failure.
Philips Ultrasound, Inc. is recalling 5,230 S5-1 Transducer units that were refurbished beyond their useful life. Affected devices were distributed nationwide and internationally.
Philips Ultrasound, Inc. is recalling 5,230 Philips C9-5EC Transducers that were refurbished beyond their useful life, which may compromise device performance and reliability.
Philips Ultrasound is recalling 5,230 eL18-4 ultrasound transducers that were refurbished beyond their useful life, potentially affecting device reliability.