Philips Ultrasound, Inc: Transducer, Ultrasonic, Diagnostic
Philips Ultrasound, Inc. is recalling the L17-5 Ultrasound Transducer distributed nationwide across all U.S. states to clarify labeling that defines how long the device can be safely used. This is a Class II recall, meaning there is a potential health risk but not an immediate life-threatening situation. The recall affects medical facilities and providers who use this ultrasound transducer.
- Recalling firm
- Philips Ultrasound, Inc
- Product
- Philips L17-5 Ultrasound Transducer
- Reason
- To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2025-09-05
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/2c37de18-1e96-4662-ba4c-7ded47b84003