FDA Device recall Z-2063-2025
Philips VL13-5 Transducer
- FDA Device
- Class II
- ongoing
- Published 2025-07-09
On 2025-07-09 the FDA classified a Class II recall of Philips VL13-5 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-2063-2025 |
| 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 VL13-5 Transducer.
Reason
Ultrasound transducer devices were refurbished beyond their useful life.
Identifiers
| code_info | Model No. 989605409592, 989605372211, 989605372213; UDI: (01)00884838061606(21)B1C23Z, (01)00884838061606(21)B252D4, (0…Model No. 989605409592, 989605372211, 989605372213; UDI: (01)00884838061606(21)B1C23Z, (01)00884838061606(21)B252D4, (01)00884838061606(21)B12ZWV, (01)00884838061606(21)B12QQC, (01)00884838061606(21)B23P58, (01)00884838061606(21)B0X3RL, (01)00884838061606(21)B12RN0, (01)00884838061606(21)B13BCL, (01)00884838061606(21)B1F233, (01)00884838061606(21)B2DWNC, (01)00884838061606(21)B12RN4, (01)00884838061606(21)B12ZTJ, (01)00884838061606(21)B1XR83, (01)00884838061606(21)B13DFT, (01)00884838061606(21)B12QVB, (01)00884838061606(21)B18LZX, (01)00884838067493(21)03FNNG, (01)00884838067493(21)038VY0, (01)00884838067493(21)03926P, (01)00884838067493(21)0367GM, (01)00884838067493(21)036BRP; Serial No. B1C23Z, B252D4, B12ZWV, B12QQC, B23P58, B0X3RL, B12RN0, B13BCL, B1F233, B2DWNC, B12RN4, B12ZTJ, B1XR83, B13DFT, B12QVB, B18LZX, 03FNNG, 038VY0, 03926P, 0367GM, 0399WM, 036BRP, 039250. |
|---|
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-2063-2025%22
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