Reported Sep 3, 2025 · Ongoing
X3-1 Transducer Probe
Philips Ultrasound, Inc.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.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?
- X3-1 Transducer Probe
- Lot codes and dates
Model No. 98960538810121715A
- UDI
N/ASerial No. 02YHPN02JK1H
- Amount recalled
- 171,322 units
This recall covers 69 products
The agency filed one notice per product. You are reading one of them; the other 68 are below.
56 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
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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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