FDA Device recall Z-2350-2025
C10-3v Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of C10-3v 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-2350-2025 |
| 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
C10-3v Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605409562, 989605438521, 989605381661, 989605381663, 989605398231, 989605381662, 989605409561, 98960545517…Model No. 989605409562, 989605438521, 989605381661, 989605381663, 989605398231, 989605381662, 989605409561, 989605455171, 989605492481, 989605414531, 989605406772, 989605439232, 21781A, 989606708921, 989605406771, 989605414122; UDI: (01)00884838061583(21)B1ZPMG, (01)00884838061583(21)B3GL7D, (01)00884838061583(21)B3PJJ1, 010088483806158321F021FV, (01)00884838061583(21)B1R004, (01)00884838061583(21)B389HT, (01)00884838061583(21)B39YJ9, 010088483806158321F0GK85, 010088483806158321F0GK89, (01)00884838061583(21)B3C63X, (01)00884838061583(21)B3JDTZ, (01)00884838061583(21)B1QZX2, (01)00884838061583(21)F0LCKP, (01)00884838061583(21)B2K0BP, (01)00884838061583(21)B2NJN9, (01)00884838061583(21)F03XLP, (01)00884838061583(21)F0433X, (01)00884838061583(21)F055TN, (01)00884838061583(21)F05P66, (01)00884838061583(21)F0CK3H, (01)00884838061583(21)F0LFY4, (01)00884838061583(21)F0BJLL, (01)00884838061583(21)F0JL72, (01)00884838061583(21)F0JPYV, (01)00884838061583(21)B34LHZ, (01)00884838061583(21)F04VQ5 |
|---|
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-2350-2025%22
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