Reported Jul 9, 2025 · Ongoing

Philips V6-2 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 V6-2 Transducer.
Lot codes and dates
    • Model No. 989605357563
    • 989605415042
    • 989605437982
    • 989605387201
    • 989605357561
  • UDI

    330 of 330 codes

    • (01)00884838061651(21)B1F8BF
    • (01)00884838061798(21)036HF1
    • (01)00884838061651(21)B1MB1Y
    • (01)00884838061651(21)B1P7X7
    • (01)00884838061651(21)B20WDH
    • (01)00884838061460(21)B1CYQ2
    • (01)00884838061460(21)B0ZP1G
    • (01)00884838061460(21)B0GX06
    • (01)00884838061460(21)B0T41B
    • (01)00884838061651(21)B1RYY9
    • (01)00884838061651(21)B20X2D
    • (01)00884838061460(21)B1K7CX
    • (01)00884838061798(21)036GQH
    • (01)00884838061798(21)036QQF
    • (01)00884838061798(21)B0K8G6
    • (01)00884838061798(21)B0NLYT
    • (01)00884838061798(21)03GKBK
    • (01)00884838061798(21)03CDKW
    • (01)00884838061798(21)031PP2
    • (01)00884838061798(21)B0JJ3P
    • (01)00884838061798(21)B09HK1
    • (01)00884838061798(21)0397KL
    • (01)00884838061798(21)036ZPK
    • (01)00884838061798(21)036QR2
    • (01)00884838061798(21)02Y05W
    • (01)00884838061798(21)03BVQR
    • (01)00884838061798(21)02WV2J
    • (01)00884838061798(21)0305DR
    • (01)00884838061798(21)03933Q
    • (01)00884838061798(21)038TQR
    • (01)00884838061798(21)02W80R
    • (01)00884838061798(21)B0GYV9
    • (01)00884838061798(21)03H3XM
    • (01)00884838061798(21)03CCG5
    • (01)00884838061798(21)031T4C
    • (01)00884838061798(21)036YYJ
    • (01)00884838061651(21)B0K8C4
    • (01)00884838061798(21)036H1C
    • (01)00884838061798(21)0365ZV
    • (01)00884838061798(21)036WXV
    • (01)00884838061798(21)02Z1TZ
    • (01)00884838061798(21)032C2R
    • (01)00884838061798(21)031V8K
    • (01)00884838061798(21)03CBP2
    • (01)00884838061798(21)038WHD
    • (01)00884838061798(21)036ZPJ
    • (01)00884838061798(21)031N36
    • (01)00884838061798(21)02W4HK
    • (01)00884838061798(21)B07Y9V
    • (01)00884838061798(21)034GRX
    • (01)00884838061798(21)0397R3
    • (01)00884838061798(21)0323VN
    • (01)00884838061798(21)03363L
    • (01)00884838061798(21)03939D
    • (01)00884838061798(21)033F0F
    • (01)00884838061798(21)035J0G
    • (01)00884838061798(21)02WB9Z
    • (01)00884838061798(21)038ZGT
    • (01)00884838061798(21)B04HP6
    • (01)00884838061798(21)02Z87V
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, 6:20 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.