Reported Jul 9, 2025 · Ongoing

Philips S7-2 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 S7-2 Transducer.
Lot codes and dates
    • Model No. 989605440772
    • 989605440771
    • 989803002261
  • UDI

    266 of 266 codes

    • (01)00884838067646(21)032MLP
    • (01)00884838067646(21)B1MMJ8
    • (01)00884838067646(21)02M708
    • (01)00884838067646(21)02Q7XJ
    • (01)00884838067646(21)03CX7R
    • (01)00884838067646(21)031FV7
    • (01)00884838067646(21)03C7PW
    • (01)00884838067646(21)02MJXP
    • (01)00884838067646(21)02MD57
    • (01)00884838067646(21)B07FCJ
    • (01)00884838067646(21)037HLQ
    • (01)00884838067646(21)B0D3FH
    • (01)00884838067646(21)031CCH
    • (01)00884838067646(21)B0M2ZJ
    • (01)00884838067646(21)039TX5
    • (01)00884838067646(21)02P5NP
    • (01)00884838067646(21)031KD1
    • (01)00884838067646(21)039J9F
    • (01)00884838067646(21)B0X1K1
    • (01)00884838067646(21)B0X19Q
    • (01)00884838067646(21)B04LKL
    • (01)00884838067646(21)B02VFV
    • (01)00884838067646(21)03C76J
    • (01)00884838067646(21)0377MN
    • (01)00884838067646(21)02Q81T
    • (01)00884838067646(21)032KCR
    • (01)00884838067646(21)037HKZ
    • (01)00884838067646(21)02YH4N
    • (01)00884838067646(21)02ZTV7
    • (01)00884838067646(21)B03N8W
    • (01)00884838067646(21)B0JF6L
    • (01)00884838067646(21)02VPXJ
    • (01)00884838067646(21)02MJ8V
    • (01)00884838067646(21)039GDN
    • (01)00884838067646(21)B02VM7
    • (01)00884838067646(21)03G2YM
    • (01)00884838067646(21)03C229
    • (01)00884838067646(21)03408Y
    • (01)00884838067646(21)B14389
    • (01)00884838067646(21)037FG5
    • (01)00884838067646(21)03C22H
    • (01)00884838067646(21)0360L6
    • (01)00884838067646(21)02VYX4
    • (01)00884838067646(21)038ND8
    • (01)00884838067646(21)03CTXP
    • (01)00884838067646(21)038HV0
    • (01)00884838067646(21)03H8P2
    • (01)00884838067646(21)B0D3CJ
    • (01)00884838067646(21)02M8VJ
    • (01)00884838067646(21)032KM9
    • (01)00884838067646(21)02ZXMD
    • (01)00884838067646(21)032ML8
    • (01)00884838067646(21)B0M2Y7
    • (01)00884838067646(21)03G4H4
    • (01)00884838067646(21)B04LHQ
    • (01)00884838067646(21)B03N5M
    • (01)00884838067646(21)039Q24
    • (01)00884838067646(21)035ZRG
    • (01)00884838067646(21)B0D3K6
    • (01)00884838067646(21)03C7QF
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.

Free recall alerts

Get alerted about new Philips Ultrasound, Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:43 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.