Philips Ultrasound, Inc 2025-07-09 Health serious FDA
Health · FDA · Recall #FDA-Z-2051-2025
Philips C9-5EC Transducer. Recall
Issued July 9, 2025 · Philips Ultrasound, Inc
In July 2025, Philips Ultrasound, Inc recalled the Philips C9-5EC Transducer., a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Ultrasound transducer devices were refurbished beyond their useful life.
What you should do
- 1 Stop using Philips C9-5EC Transducer. 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
- July 9, 2025
- Units affected
- Not reported
- Sold at
- Domestic: Nationwide Distribution; Foreign: Australia, Austria, Belgium, Brazil, Bulgaria, Canada, Chile, China, Colombia, Czech Republic, D
- Recall number
- FDA-Z-2051-2025
- 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.