Philips Ultrasound Transducer C10-3v Probe Labeling Clarification Recall
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.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: This Class III recall addresses a documentation and labeling issue regarding product useful life. No hazards, illnesses, or injuries are reported. Class III recalls involving documentation clarification are typically scored as low severity per the rubric.
Plain-English summary
Philips Ultrasound, Inc. is recalling the Transducer C10-3v Transducer Probe. The recall affects 171,322 units distributed nationwide in the United States.
The purpose of this recall is to provide clarification and labeling to define the useful life of ultrasound transducers in the field. The FDA has classified this as a Class III recall.
Users of affected transducers should contact Philips Ultrasound, Inc. for updated labeling and documentation regarding the product's useful life.
The recalled product
- Product
- Transducer C10-3v Transducer Probe
- Manufacturer
- Philips Ultrasound, Inc
- Hazard
- labeling-deficiency
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- Model No. N/A
- UDI: N/A
- Serial No. B2WXV7.
Distribution
Distributed nationwide across the United States.
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