FDA Device recall Z-2065-2025
Philips X6-1 Transducer
- FDA Device
- Class II
- ongoing
- Published 2025-07-09
On 2025-07-09 the FDA classified a Class II recall of Philips X6-1 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-2065-2025 |
| 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 X6-1 Transducer.
Reason
Ultrasound transducer devices were refurbished beyond their useful life.
Identifiers
| code_info | Model No. 989605409282, 989605438511, 989605357143, 989605357141; UDI: (01)00884838061446(21)B1HT1C, (01)00884838061446…Model No. 989605409282, 989605438511, 989605357143, 989605357141; UDI: (01)00884838061446(21)B1HT1C, (01)00884838061446(21)B1HT47, (01)00884838061446(21)B1W368, (01)00884838061446(21)B1WBDL, (01)00884838061446(21)B1GTFL, (01)00884838061446(21)B11YW3, (01)00884838061446(21)B15QX1, (01)00884838061446(21)B14LVN, (01)00884838061446(21)B22R48, (01)00884838061446(21)B11XQP, (01)00884838061446(21)B1HTJ3, (01)00884838061446(21)B11Z3B, (01)00884838061446(21)B0WX2W, (01)00884838061446(21)B0WYZ1, (01)00884838061446(21)B131LH, (01)00884838061446(21)B1C1C3, (01)00884838061446(21)B1JBBF, (01)00884838061446(21)B101WK, (01)00884838061446(21)B14M20, (01)00884838061446(21)B1GVWH, (01)00884838061446(21)B1H6V3, (01)00884838061446(21)B101TF, (01)00884838061446(21)B1JCYV, (01)00884838061446(21)B2HQD0, (01)00884838061446(21)B27YP9, (01)00884838061446(21)B21DZ3, (01)00884838061446(21)B0Z7G7, (01)00884838061446(21)B0V082, (01)00884838061446(21)B22QVL, (01)00884838061446(21)B14MMW, (01)00884838061446(21)B24VGG, |
|---|
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-2065-2025%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.