FDA Device recall Z-2367-2025
D2TCD Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of D2TCD 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-2367-2025 |
| 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
D2TCD Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605412102, 989605438591; UDI: (01)00884838061361(21)B1N4HT, (01)00884838061361(21)B1N4J6, (01)008848380613…Model No. 989605412102, 989605438591; UDI: (01)00884838061361(21)B1N4HT, (01)00884838061361(21)B1N4J6, (01)00884838061361(21)B2L6QZ, (01)00884838061361(21)B2L6R0, (01)00884838061361(21)B2L6T9, (01)00884838061361(21)F01C9Y, (01)00884838061361(21)F074NX, (01)00884838061361(21)B2Q7FK, (01)00884838061361(21)F08MVZ, (01)00884838061361(21)B1NDJD, (01)00884838061361(21)B1N4JF, (01)00884838061361(21)B2L6TV, (01)00884838061361(21)F05Z77, (01)00884838061361(21)B2Q71X, (01)00884838061361(21)F0998F, (01)00884838061361(21)F0998J, (01)00884838061361(21)F09WC4, (01)00884838061361(21)F02H8Q, (01)00884838061361(21)F07JPJ, (01)00884838061361(21)F00LFM, (01)00884838061361(21)F00LFN, (01)00884838061361(21)B2Q7FT, (01)00884838061361(21)B2L6RJ, (01)00884838061361(21)B2L6RF, (01)00884838061361(21)B1N4KJ, (01)00884838061361(21)F067C1, (01)00884838061361(21)F068GD, (01)00884838061361(21)B1N4JR, (01)00884838061361(21)B2Q7FZ, (01)00884838061361(21)F01J0W, (01)00884838061361(21)B2Q71V, (01)00884838061361(21)B2Q71 |
|---|
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-2367-2025%22
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