Reported Jul 9, 2025 · Ongoing

Philips X7-2t 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 X7-2t Transducer.
Lot codes and dates
    • Model No. 989605350454
    • 989605361911
    • 989605414122
    • 989605461941
    • 989605350452
    • 989605350451
    • 989605455171
    • 989605350453
    • 989605438611
  • UDI

    1,082 of 1,082 codes

    • Unique Device Identifier (UDI)
    • (01)00884838061668(21)B144RL
    • (01)00884838061668(21)B28L3F
    • (01)00884838061668(21)B26MZ9
    • (01)00884838061668(21)B3DT21
    • (01)00884838061668(21)B3DP0K
    • (01)00884838061668(21)B2JJFV
    • (01)00884838061668(21)B0T9J4
    • (01)00884838061668(21)B2XCH6
    • (01)00884838061668(21)B3DRBG
    • (01)00884838061668(21)B21DC0
    • (01)00884838061668(21)B21C1Q
    • (01)00884838061668(21)B13R5Z
    • (01)00884838061668(21)B2JJM6
    • (01)00884838061668(21)B2JJ71
    • (01)00884838061668(21)B1ZGT3
    • (01)00884838061668(21)B1C112
    • (01)00884838061668(21)B1JMPG
    • (01)00884838061668(21)B1ZH27
    • (01)00884838061668(21)B1XZ2L
    • (01)00884838061668(21)B3DT3K
    • (01)00884838061668(21)B20TVK
    • (01)00884838061668(21)B1BDJG
    • (01)00884838061668(21)B1TY40
    • (01)00884838061668(21)B1ZGM3
    • (01)00884838061668(21)B1J660
    • (01)00884838061668(21)B1TCB5
    • (01)00884838061668(21)B238J6
    • (01)00884838061668(21)B2VQN4
    • (01)00884838061668(21)B1ZH4K
    • (01)00884838061668(21)B191TJ
    • (01)00884838061668(21)B21DL6
    • (01)00884838061668(21)B1TB82
    • (01)00884838061668(21)B23F6J
    • (01)00884838061668(21)B15PQH
    • (01)00884838061668(21)B22VHF
    • (01)00884838061668(21)B110QK
    • (01)00884838061668(21)B1W3GK
    • (01)00884838061668(21)B1HCHJ
    • (01)00884838061668(21)B1ZGYV
    • (01)00884838061668(21)B3M1H8
    • (01)00884838061668(21)B1W32L
    • (01)00884838061668(21)B18B6P
    • (01)00884838061668(21)B2VQ9X
    • (01)00884838061668(21)B20TTV
    • (01)00884838061668(21)B1HD2N
    • (01)00884838061668(21)B15TH2
    • (01)00884838061668(21)B0Z86G
    • (01)00884838061668(21)B1TB7R
    • (01)00884838061668(21)B2XCHX
    • (01)00884838061668(21)B13Q48
    • (01)00884838061668(21)B1J74Z
    • (01)00884838061668(21)B18B6N
    • (01)00884838061668(21)B1JG1W
    • (01)00884838061668(21)B1FFTG
    • (01)00884838061668(21)B21DDR
    • (01)00884838061668(21)B18CFL
    • (01)00884838061668(21)B17G4Y
    • (01)00884838061668(21)B1VZRG
    • (01)00884838061668(21)B1ZD3H
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, 5:41 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.