FDA Device recall Z-2062-2025
Philips V6-2 Transducer
- FDA Device
- Class II
- ongoing
- Published 2025-07-09
On 2025-07-09 the FDA classified a Class II recall of Philips V6-2 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-2062-2025 |
| 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 V6-2 Transducer.
Reason
Ultrasound transducer devices were refurbished beyond their useful life.
Identifiers
| code_info | Model No. 989605357563, 989605415042, 989605437982, 989605387201, 989605357561; UDI: (01)00884838061651(21)B1F8BF, (01)…Model No. 989605357563, 989605415042, 989605437982, 989605387201, 989605357561; UDI: (01)00884838061651(21)B1F8BF, (01)00884838061798(21)036HF1, (01)00884838061651(21)B1MB1Y, (01)00884838061651(21)B1P7X7, (01)00884838061651(21)B20WDH, (01)00884838061460(21)B1CYQ2, (01)00884838061460(21)B0ZP1G, (01)00884838061460(21)B0GX06, (01)00884838061460(21)B0T41B, (01)00884838061651(21)B1RYY9, (01)00884838061651(21)B20X2D, (01)00884838061460(21)B1K7CX, (01)00884838061798(21)036GQH, (01)00884838061798(21)036QQF, (01)00884838061798(21)B0K8G6, (01)00884838061798(21)B0NLYT, (01)00884838061798(21)03GKBK, (01)00884838061798(21)03CDKW, (01)00884838061798(21)031PP2, (01)00884838061798(21)B0JJ3P, (01)00884838061798(21)B09HK1, (01)00884838061798(21)0397KL, (01)00884838061798(21)036ZPK, (01)00884838061798(21)036QR2, (01)00884838061798(21)02Y05W, (01)00884838061798(21)03BVQR, (01)00884838061798(21)02WV2J, (01)00884838061798(21)0305DR, (01)00884838061798(21)03933Q, (01)00884838061798(21)038TQR, (01)00884838061 |
|---|
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-2062-2025%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.