FDA Device recall Z-2058-2025
Philips S5-1 Transducer
- FDA Device
- Class II
- ongoing
- Published 2025-07-09
On 2025-07-09 the FDA classified a Class II recall of Philips S5-1 Transducer by Philips Ultrasound, citing ultrasound transducer devices were refurbished beyond their useful life.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2058-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-05-28 |
| Published | 2025-07-09 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips Ultrasound |
| Distribution | US |
Product
Philips S5-1 Transducer.
Reason
Ultrasound transducer devices were refurbished beyond their useful life.
Identifiers
| code_info | Model No. 989605412082, 989605440682, 989605440681, 989803002101; UDI: (01)00884838061637(21)B1FTT9, (01)0088483806163…Model No. 989605412082, 989605440682, 989605440681, 989803002101; UDI: (01)00884838061637(21)B1FTT9, (01)00884838061637(21)B18351, (01)00884838061637(21)B1F61P, (01)00884838061637(21)B13G8Q, (01)00884838061637(21)B1F8HC, (01)00884838061637(21)B13G72, (01)00884838061637(21)B15D2R, (01)00884838061637(21)B0R53Y, (01)00884838061637(21)B15CCP, (01)00884838061637(21)B194WG, (01)00884838061637(21)B0ZZF8, (01)00884838061637(21)B15NQ6, (01)00884838061637(21)B170FW, (01)00884838061637(21)B15P4B, (01)00884838061637(21)B0QNTP, (01)00884838061637(21)B140K4, (01)00884838061637(21)B10JZD, (01)00884838061637(21)B15P33, (01)00884838061637(21)B1BGV2, (01)00884838061637(21)B1951N, (01)00884838061637(21)B0R4FP, (01)00884838061637(21)B0R534, (01)00884838061637(21)B10QPH, (01)00884838061637(21)B1PBWF, (01)00884838061637(21)B15D10, (01)00884838061637(21)B16X3N, (01)00884838061637(21)B18VVZ, (01)00884838061637(21)B1L28V, (01)00884838061637(21)B1KY4P, (01)00884838061637(21)B0XB7F, (01)00884838061637(21)B0R40C |
|---|
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-2058-2025%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.