Reported Jul 9, 2025 · Ongoing

Philips S8-3t 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 S8-3t Transducer.
Lot codes and dates
    • Model No. 989605420183
    • 989605431171
    • 989605439232
    • 989605406772
    • 989605439231
    • 989606708921
    • 989803002661
  • UDI

    477 of 477 codes

    • (01)00884838073524(21)B2HWZ5
    • (01)00884838073524(21)B34PCJ
    • (01)00884838073524(21)B34PBW
    • (01)00884838073524(21)B37JHN
    • (01)00884838073524(21)B34P9K
    • (01)00884838073524(21)B2106G
    • (01)00884838073524(21)B210DC
    • (01)00884838073524(21)B2101L
    • (01)00884838073524(21)B2HX89
    • (01)00884838073524(21)B2HX1G
    • (01)00884838073524(21)B2HX7N
    • (01)00884838073524(21)B2HXBB
    • (01)00884838073524(21)B2HWZ6
    • (01)00884838073524(21)B2HXB8
    • (01)00884838073524(21)B2HX1D
    • (01)00884838073524(21)B2HWXV
    • (01)00884838073524(21)B209LJ
    • (01)00884838073524(21)B37JHP
    • (01)00884838073524(21)B2HWXW
    • (01)00884838073524(21)B2105P
    • (01)00884838073524(21)B1Z0Z8
    • (01)00884838073524(21)B210D8
    • (01)00884838073524(21)B21004
    • (01)00884838073524(21)B1Z0ZD
    • (01)00884838073524(21)B2HXDN
    • (01)00884838067523(21)B0XTVJ
    • (01)00884838073524(21)B2HWXX
    • (01)00884838073524(21)B20ZYV
    • (01)00884838073524(21)B2HWWW
    • (01)00884838073524(21)B2HBQR
    • (01)00884838073524(21)B2HXK7
    • (01)00884838073524(21)B2109B
    • (01)00884838073524(21)B2HXDQ
    • (01)00884838073524(21)B2109V
    • (01)00884838073524(21)B34PGV
    • (01)00884838073524(21)B2107T
    • (01)00884838073524(21)B34PGQ
    • (01)00884838073524(21)B3DVD7
    • (01)00884838073524(21)B34PB8
    • (01)00884838073524(21)B3DV8N
    • (01)00884838073524(21)B2100W
    • (01)00884838073524(21)B21047
    • (01)00884838073524(21)B2109H
    • (01)00884838073524(21)B2HXG0
    • (01)00884838073524(21)B2HX3K
    • (01)00884838073524(21)B209LK
    • (01)00884838073524(21)B2HBR9
    • (01)00884838073524(21)B2HWZB
    • (01)00884838073524(21)B2105N
    • (01)00884838073524(21)B2101B
    • (01)00884838073524(21)B3DV7H
    • (01)00884838073524(21)B2106X
    • (01)00884838073524(21)B2HX7M
    • (01)00884838073524(21)B2HXB9
    • (01)00884838073524(21)B34P81
    • (01)00884838067523(21)B0JX0K
    • (01)00884838073524(21)B2HWWT
    • (01)00884838067530(21)B0PRPT
    • (01)00884838061439(21)B11X0W
    • (01)00884838067530(21)B157Q6
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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:40 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.