FDA Device recall Z-2355-2025
C6-2 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of C6-2 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-2355-2025 |
| 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
C6-2 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605418982, 989605418983, 989605463391, 989605463391, 989605442151, 989605387071, 989605418972; UDI: (01)00…Model No. 989605418982, 989605418983, 989605463391, 989605463391, 989605442151, 989605387071, 989605418972; UDI: (01)00884838067868(21)B1N309, (01)00884838067868(21)B1N3GM, (01)00884838067868(21)B20LH9, (01)00884838087163(21)B27M92, (01)00884838087163(21)B2D4X5, (01)00884838087163(21)B2TQDL, (01)00884838087163(21)B2TQHL, (01)00884838087163(21)B2TR9L, (01)00884838087163(21)B2TR9R, (01)00884838087163(21)B32NLQ, (01)00884838087163(21)B32P57, (01)00884838087163(21)B3WW8C, (01)00884838087163(21)B40ZK4, (01)00884838087163(21)F05J29, (01)00884838087163(21)F0GGQZ, (01)04719873000036(21)B2TR3Y, (01)04719873000036(21)B3HZ2G, (01)04719873000036(21)F08334, (01)04719873000036(21)F0H6X0, 010088483808716321B3XNQK, 010471987300003621B2D52G, (01)00884838067868(21)B27KQ5, (01)00884838087163(21)F08BN7, (01)00884838067868(21)B1N327, (01)00884838067868(21)B1N35V, (01)00884838087163(21)B2THXY, (01)00884838087163(21)B2TJ1M, (01)00884838087163(21)B2ZMG6, (01)04719873000036(21)B3TKBZ, (01)04719873000036(21)B3W |
|---|
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-2355-2025%22
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