Philips Ultrasound, Inc 2025-09-03 Health moderate FDA
Health · FDA · Recall #FDA-Z-2402-2025
TRANSDUCER L12-5 Transducer Probe Recall
Issued September 3, 2025 · Philips Ultrasound, Inc
In September 2025, Philips Ultrasound, Inc recalled the TRANSDUCER L12-5 Transducer Probe, a moderate health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
What you should do
- 1 Stop using TRANSDUCER L12-5 Transducer Probe right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Philips Ultrasound, Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Philips Ultrasound, Inc
- Category
- Health
- Recall date
- September 3, 2025
- Units affected
- Not reported
- Sold at
- US Nationwide distribution.
- Recall number
- FDA-Z-2402-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Philips Ultrasound, Inc has 11 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.