FDA Device recall Z-2056-2025
Philips L8-4 Transducer
- FDA Device
- Class II
- ongoing
- Published 2025-07-09
On 2025-07-09 the FDA classified a Class II recall of Philips L8-4 Transducer by Philips Ultrasound, citing ultrasound transducer devices were refurbished beyond their useful life.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2056-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-05-28 |
| Published | 2025-07-09 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips Ultrasound |
| Distribution | US |
Product
Philips L8-4 Transducer.
Reason
Ultrasound transducer devices were refurbished beyond their useful life.
Identifiers
| code_info | Model No. 989605440811, 989605440812; UDI: (01)00884838067684(21)B0LZNN, (01)00884838067684(21)03BPVM, (01)008848380676…Model No. 989605440811, 989605440812; UDI: (01)00884838067684(21)B0LZNN, (01)00884838067684(21)03BPVM, (01)00884838067684(21)02KMFZ, (01)00884838067684(21)02HJDK, (01)00884838067684(21)02FWNQ, (01)00884838067684(21)02KKZT, (01)00884838067684(21)03H7GL, (01)00884838067684(21)02LTKK, (01)00884838067684(21)02H2JM, (01)00884838067684(21)02KKVB, (01)00884838067684(21)038XYV, (01)00884838067684(21)02DLVR, (01)00884838067684(21)02CCM5, (01)00884838067684(21)02LT6G, (01)00884838067684(21)02KMKK, (01)00884838067684(21)02V8VD, (01)00884838067684(21)037Z2B, (01)00884838067684(21)02NK5J; Serial No. B0LZNN, 03BPVM, 02KMFZ, 02HJDK, 02KLBP, 02FWNQ, 02RTF9, 02KKZT, 03H7GL, 02LTKK, 02H2JM, 02KKVB, 038XYV, 02H34T, 02DLVR, 02CCM5, 02LT6G, 02KMKK, 02V8VD, 02JC66, 02V016, 037Z2B, 02NK5J. |
|---|
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-2056-2025%22
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