FDA Device recall Z-2059-2025
Philips S7-2 Transducer
- FDA Device
- Class II
- ongoing
- Published 2025-07-09
On 2025-07-09 the FDA classified a Class II recall of Philips S7-2 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-2059-2025 |
| 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 S7-2 Transducer.
Reason
Ultrasound transducer devices were refurbished beyond their useful life.
Identifiers
| code_info | Model No. 989605440772, 989605440771, 989803002261; UDI: (01)00884838067646(21)032MLP, (01)00884838067646(21)B1MMJ8, (0…Model No. 989605440772, 989605440771, 989803002261; UDI: (01)00884838067646(21)032MLP, (01)00884838067646(21)B1MMJ8, (01)00884838067646(21)02M708, (01)00884838067646(21)02Q7XJ, (01)00884838067646(21)03CX7R, (01)00884838067646(21)031FV7, (01)00884838067646(21)03C7PW, (01)00884838067646(21)02MJXP, (01)00884838067646(21)02MD57, (01)00884838067646(21)B07FCJ, (01)00884838067646(21)037HLQ, (01)00884838067646(21)B0D3FH, (01)00884838067646(21)031CCH, (01)00884838067646(21)B0M2ZJ, (01)00884838067646(21)039TX5, (01)00884838067646(21)02P5NP, (01)00884838067646(21)031KD1, (01)00884838067646(21)039J9F, (01)00884838067646(21)B0X1K1, (01)00884838067646(21)B0X19Q, (01)00884838067646(21)B04LKL, (01)00884838067646(21)B02VFV, (01)00884838067646(21)03C76J, (01)00884838067646(21)0377MN, (01)00884838067646(21)02Q81T, (01)00884838067646(21)032KCR, (01)00884838067646(21)037HKZ, (01)00884838067646(21)02YH4N, (01)00884838067646(21)02ZTV7, (01)00884838067646(21)B03N8W, (01)00884838067646(21)B0JF6L, (01)008848380 |
|---|
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-2059-2025%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.