FDA Device recall Z-2382-2025
L9-3 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of L9-3 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-2382-2025 |
| 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
L9-3 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605387361, 989605353303, 989605353301, 989605365003; UDI: (01)00884838061767(21)B3PV40, (01)00884838061767…Model No. 989605387361, 989605353303, 989605353301, 989605365003; UDI: (01)00884838061767(21)B3PV40, (01)00884838061767(21)B3JRCQ, (01)00884838061767(21)B1ZRXY, (01)00884838061767(21)B1ZRY3, (01)00884838061767(21)B2G5L6, (01)00884838061767(21)B2JFF8, (01)00884838061767(21)B2JZ26, (01)00884838061767(21)B2R3XW, (01)00884838061767(21)B2Y7FN, (01)00884838061767(21)B2YD2P, (01)00884838061767(21)B33XHX, (01)00884838061767(21)B37VC0, (01)00884838061767(21)B2RLWL, (01)00884838061767(21)B3NT2M, (01)00884838061767(21)B2KLVJ, (01)00884838061767(21)B2JF6F, (01)00884838061767(21)B2Y53M, (01)00884838061767(21)B2T51H, (01)00884838061767(21)B3JWZB, (01)00884838061767(21)B3RJ6B, (01)00884838061767(21)B3VBQP, (01)00884838061767(21)B2LL7Z, (01)00884838061767(21)B2Y7BL, (01)00884838061767(21)B22LK7, (01)00884838061767(21)B29JNQ, (01)00884838061767(21)B31CCC, (01)00884838061767(21)B3C6BP, (01)00884838061767(21)B3JRLK, (01)00884838061767(21)B2YNBX, (01)00884838061767(21)B1YQBZ, (01)00884838061767(21)B2ZBZC, |
|---|
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-2382-2025%22
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