FDA Device recall Z-2352-2025
c5-1 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of c5-1 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-2352-2025 |
| 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
c5-1 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605412042, 989605438541, 989605388071, 989605365003, 989605365001, 989605366331, 989605387852, 98960536500…Model No. 989605412042, 989605438541, 989605388071, 989605365003, 989605365001, 989605366331, 989605387852, 989605365004, 989605492481, 989605431531, 989605412072, 989606702251, 989605391092, 989605353303, 989605418552, 989605455171, 989605412041; UDI: (01)00884838061491(21)B2JTQ2, (01)00884838061507(21)B2KPHY, (01)00884838061613(21)B0TN11, (01)00884838061613(21)B0WPLV, (01)00884838061613(21)B0ZVFL, (01)00884838061613(21)B126WZ, (01)00884838061613(21)B13K7V, (01)00884838061613(21)B1434L, (01)00884838061613(21)B14QMX, (01)00884838061613(21)B16ZF8, (01)00884838061613(21)B17161, (01)00884838061613(21)B173X2, (01)00884838061613(21)B1743J, (01)00884838061613(21)B1811G, (01)00884838061613(21)B1C20X, (01)00884838061613(21)B1C5K5, (01)00884838061613(21)B1C764, (01)00884838061613(21)B1DT4H, (01)00884838061613(21)B1DXHY, (01)00884838061613(21)B1FDZ9, (01)00884838061613(21)B1K2G0, (01)00884838061613(21)B1K7F0, (01)00884838061613(21)B1LCZW, (01)00884838061613(21)B1LHJ3, (01)00884838061613(21)B1LHW |
|---|
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-2352-2025%22
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