Reported Jul 9, 2025 · Ongoing
Philips XL14-3 Transducer.
Philips Ultrasound, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Philips Ultrasound, Inc · 1 Echo Dr · Reedsville, PA · 17084-8603
Is this the product you have?
- Philips XL14-3 Transducer.
- Lot codes and dates
- Model No. 989605409251
- UDI
(01)00884838074613(21)B1ZL08Serial No. B1ZL08
- Amount recalled
- 5,230 units
This recall covers 21 products
The agency filed one notice per product. You are reading one of them; the other 20 are below.
8 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Ultrasound transducer devices were refurbished beyond their useful life.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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