Reported Jul 9, 2025 · Ongoing
Philips L9-3 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 L9-3 Transducer.
- Lot codes and dates
Model No. 989605353301989605353303989605387361
- UDI
N/ASerial No. B0ZTD103F40C03923H0314BQ03712H033HGC03CJ9M035JY003CFTH0399XP030FNL037R8102ZH610358PF033JGV03FN8203230B03145Y02XYB302XWH402Z1D903591C0359Q103598Y035JVM02WVF002WYT103CFPG02XWN102ZJR602NV7G0305WC036XY302XY9D03FNPD02ZJPHB08PVN0373HXB0NP6L03F36403922W02X17302WYQX02ND560367GW0315P302QMTL038W7203315L0358PV033JK703128V032297
- 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.
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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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