FDA Device recall Z-2396-2025
S7-2t Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of S7-2t 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-2396-2025 |
| 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
S7-2t Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 21778A, 989605440772; UDI: (01)00884838067646(21)B199HC, (01)00884838067646(21)B20ZV2, (01)00884838067646(21)…Model No. 21778A, 989605440772; UDI: (01)00884838067646(21)B199HC, (01)00884838067646(21)B20ZV2, (01)00884838067646(21)B1MMLZ, (01)00884838067646(21)B04LQ0, (01)00884838067646(21)B20ZW6, (01)00884838067646(21)B0X1HK, (01)00884838067646(21)B199CY, (01)00884838067646(21)B02VM7, (01)00884838067646(21)B0X1KX, (01)00884838067646(21)B1MMLD, (01)00884838067646(21)B20ZT7, (01)00884838067646(21)B1MMK0, (01)00884838067646(21)B2JGW0, (01)00884838067646(21)B20ZVC, (01)00884838067646(21)B199DH, (01)00884838067646(21)B1MMJM, (01)00884838067646(21)B1MMH3, (01)00884838067646(21)B20ZWB, (01)00884838067646(21)B1MMLY, (01)00884838067646(21)B14389, (01)00884838067646(21)B1MMH4, (01)00884838067646(21)B20ZWK, (01)00884838067646(21)B1MMJZ, (01)00884838067646(21)B1MMKN, (01)00884838067646(21)B20ZT4, (01)00884838067646(21)B20ZWY, (01)00884838067646(21)B2JJ40, (01)00884838067646(21)B2JGLK, (01)00884838067646(21)B0X1LJ, (01)00884838067646(21)B1MMM4, (01)00884838067646(21)B20ZW0, (01)00884838067646(21)B199DG, (01 |
|---|
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-2396-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.