Reported Jul 9, 2025 · Ongoing

Philips L12-4 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 L12-4 Transducer.
Lot codes and dates
    • Model No. 989605427122
    • 989605451171
    • 989605434813
    • 989605434812
    • 989605477121
    • 989605434811
  • UDI

    507 of 507 codes

    • (01)00884838072305(21)B1QJ17
    • (01)00884838061644(21)B2BBRN
    • (01)00884838061644(21)B1GL69
    • (01)00884838072305(21)B1YHN7
    • (01)00884838061644(21)B186QV
    • (01)00884838072305(21)B1QJ0G
    • (01)00884838072305(21)B21GPF
    • (01)00884838072305(21)B1QJ27
    • (01)00884838072305(21)B1QJ0V
    • (01)00884838061644(21)B14YT4
    • 010088483808516921B1L72F
    • (01)00884838072305(21)B21GNP
    • (01)00884838072305(21)B21GNR
    • (01)00884838072305(21)B1YHPV
    • (01)00884838072305(21)B21GRD
    • (01)00884838072305(21)B21GMK
    • (01)00884838085169(21)B1KFNJ
    • (01)00884838085169(21)B1QGTW
    • (01)00884838085169(21)B1L78H
    • (01)00884838072305(21)B1YHNZ
    • (01)00884838072305(21)B21GQ1
    • (01)00884838072305(21)B36LQZ
    • 010088483807230521B21GP4
    • (01)00884838072305(21)B1YHNK
    • 010088483808516921B27DYL
    • (01)00884838085169(21)B1XFGG
    • (01)00884838072305(21)B21GQH
    • (01)00884838072305(21)B329WD
    • (01)00884838085169(21)B1QGXP
    • (01)00884838072305(21)B21GQ6
    • (01)00884838072305(21)B21GR5
    • (01)00884838085169(21)B1KFG2
    • (01)00884838085169(21)B1QH54
    • 010088483808516921B1KFMW
    • (01)00884838085169(21)B1L75L
    • (01)00884838085169(21)B1QH17
    • (01)00884838085169(21)B1L762
    • (01)00884838085169(21)B1JNQF
    • (01)00884838085169(21)B1QGYV
    • (01)00884838085169(21)B1L744
    • (01)00884838085169(21)B21ZCX
    • (01)00884838085169(21)B1KFL7
    • (01)00884838085169(21)B1L75N
    • (01)00884838085169(21)B23HB3
    • (01)00884838085169(21)B1L7BD
    • (01)00884838085169(21)B2Y9FR
    • (01)00884838072305(21)B21GQV
    • (01)00884838068759(21)B23GRT
    • 010088483808516921B1XF88
    • (01)00884838085169(21)B23GQV
    • (01)00884838085169(21)B27D0L
    • (01)00884838086586(21)B2C7MF
    • (01)00884838085169(21)B1L7B5
    • 010088483808516921B1QGWZ
    • (01)00884838085169(21)B1QH70
    • (01)00884838072305(21)B2D3Z2
    • (01)00884838085169(21)B27F19
    • (01)00884838085169(21)B2YBCY
    • (01)00884838085169(21)B27D22
    • (01)00884838085169(21)B23GR7
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, 6:58 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.