FDA Device recall Z-2405-2025
VL13-5 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of VL13-5 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-2405-2025 |
| 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
VL13-5 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605409592, 989605439931; UDI: (01)00884838061606(21)B2LKRC, (01)00884838061606(21)B1RY95, (01)008848380616…Model No. 989605409592, 989605439931; UDI: (01)00884838061606(21)B2LKRC, (01)00884838061606(21)B1RY95, (01)00884838061606(21)B26B50, (01)00884838061606(21)B29K57, (01)00884838061606(21)B1GK0X, (01)00884838061606(21)B285DN, (01)00884838061606(21)B285DP, (01)00884838061606(21)B2865W, (01)00884838061606(21)B2DW9V, (01)00884838061606(21)B252D1, (01)00884838061606(21)B20XP7, (01)00884838061606(21)F010PF, (01)00884838061606(21)B2865X, (01)00884838061606(21)B20YTN, (01)00884838061606(21)B21T6J, (01)00884838061606(21)B2281P, (01)00884838061606(21)B2G3L0, (01)00884838061606(21)B29DGY, (01)00884838061606(21)B285DQ, (01)00884838061606(21)B1TW50, (01)00884838061606(21)B289V9, (01)00884838061606(21)B1PK9D, (01)00884838061606(21)B1QRX1, (01)00884838061606(21)B33XYT, (01)00884838061606(21)B1QC2H; Serial No. B2LKRC, B1F5NL, B1RY95, B26B50, B29K57, B1C5HY, B1GK0X, B285DN, B285DP, B2865W, B13D9W, B1C5R3, B1F0N7, B2DW9V, B252D1, B20XP7, F010PF, B2865X, B20YTN, B21T6J, B2281P, B2G3L0, B29DGY, B285DQ, B1BN |
|---|
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-2405-2025%22
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