FDA Device recall Z-2372-2025
L12-3 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of L12-3 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-2372-2025 |
| 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
L12-3 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605412072, 989605492481, 989605438571, 989605430253, 989605348243, 989605412071, 989605366211, 98960541204…Model No. 989605412072, 989605492481, 989605438571, 989605430253, 989605348243, 989605412071, 989605366211, 989605412042, 989605387241, 989605400521, 21475A, 989605456291; UDI: (01)00884838061620(21)B1WH6H, (01)00884838061620(21)B1WK9N, (01)00884838061620(21)B2278N, (01)00884838061620(21)B2ZC90, (01)00884838061620(21)B3GLHC, (01)00884838061620(21)B3KQWJ, (01)00884838061620(21)B3RB89, (01)00884838061620(21)F0112F, (01)00884838090804(21)B3F4N0, (01)00884838090804(21)B3NJZK, (01)00884838090804(21)F04ZGP, (01)00884838090804(21)F06W70, (01)00884838090804(21)F0B5FT, (01)00884838090804(21)F0D97N, (01)00884838090804(21)F0KNM8, 010088483809080421F021KZ, 010088483809080421F023DB, (01)00884838090804(21)F0LJNK, N/A, (01)00884838061620(21)B3BTG6, (01)00884838090804(21)F0K3YK, (01)00884838061620(21)F0KJT5, (01)00884838061620(21)B1QMN8, (01)00884838061620(21)B24X8V, (01)00884838061620(21)B24XKZ, 010088483809080421F0G2BJ, (01)00884838061620(21)B20XVR, (01)00884838061620(21)F06NV0, (01)00884838061620(2 |
|---|
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-2372-2025%22
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