FDA Device recall Z-2376-2025
L12-5 50 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of L12-5 50 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-2376-2025 |
| 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
L12-5 50 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605418552, 989605408173, 989605438481, 989605420231, 989605412401, 989605408171, 989605362313, 98960539600…Model No. 989605418552, 989605408173, 989605438481, 989605420231, 989605412401, 989605408171, 989605362313, 989605396002, 989605387311, 989605412042, 989605418551, 989605409562, 989605412072, 989605409582, 989605440931, 989605361882, 989605440932; UDI: (01)00884838067851(21)B1N28J, (01)00884838067851(21)B1N2GB, (01)00884838067851(21)B20JW8, (01)00884838067851(21)B2TL6N, (01)00884838067851(21)B2TM54, (01)00884838067851(21)B2TNPZ, (01)00884838067851(21)B2TPD0, (01)00884838067851(21)B2ZJYP, (01)00884838067974(21)B24F91, (01)00884838067851(21)B2TMH2, 010088483806785121F0FNVH, 010088483806785121F0FQMW, 010088483806785121F0FQNJ, (01)00884838067851(21)B24NM7, (01)00884838067851(21)B2D9MB, (01)00884838067851(21)B2D9VH, (01)00884838067851(21)B2H8B5, (01)00884838067851(21)B2PL21, (01)00884838067851(21)B40HY0, (01)00884838067851(21)B40J43, (01)00884838067974(21)B1N1NV, (01)00884838067851(21)B3XX7R, (01)00884838067851(21)F088MN, (01)00884838067851(21)B0P7DV, (01)00884838067851(21)B2ZHQ3, (01)0088 |
|---|
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-2376-2025%22
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