FDA Device recall Z-2371-2025
L11-3 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of L11-3 Transducer Probe by Philips Ultrasound, citing to provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2371-2025 |
| Classification | Class III |
| Status | ongoing |
| Initiated | 2025-07-03 |
| Published | 2025-09-03 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips Ultrasound |
| Distribution | US |
Product
L11-3 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605388251, 989605400511, 989605400513, 989605440762; UDI: (01)00884838067639(21)B1Y3CY, (01)00884838067967…Model No. 989605388251, 989605400511, 989605400513, 989605440762; UDI: (01)00884838067639(21)B1Y3CY, (01)00884838067967(21)F08RH4, (01)00884838067639(21)B1Y33W, (01)00884838067967(21)B1X2F6, (01)00884838067639(21)B1RY1G, (01)00884838067639(21)B1RXQ9, (01)00884838067639(21)B305V2, (01)00884838067967(21)B2H0PB, (01)00884838067967(21)B2PQ4H, (01)00884838067967(21)B2GZFN, (01)00884838067967(21)B2PV1V, (01)00884838067967(21)B2PTWK, (01)00884838067967(21)B2PMRG, (01)00884838067967(21)B2PMR8, (01)00884838067967(21)F08MFD, (01)00884838067967(21)B20DKD, (01)00884838067967(21)B24Q2T, (01)00884838067967(21)B27J4W, (01)00884838067967(21)B32RQX, (01)00884838067639(21)B1Y2DB, (01)00884838067967(21)B20KMM, (01)00884838067967(21)B1WTXZ, (01)00884838067967(21)B3YNDY, (01)00884838067639(21)B1Y3FG, (01)00884838067967(21)B1RMX9, (01)00884838067639(21)B2NN5M, (01)00884838067967(21)B2ZV3F, (01)00884838067639(21)B1Y3DR, (01)00884838067967(21)B24Q31, (01)00884838067967(21)F0GJN2, (01)00884838067967(21)B2PPZ7; |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2371-2025%22
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