FDA Device recall Z-0390-2024
Achieva 1.5T Conversion
- FDA Device
- Class II
- ongoing
- Published 2023-11-29
On 2023-11-29 the FDA classified a Class II recall of Achieva 1.5T Conversion by Philips North America, citing potential component failure in the Gradient Coil could product smoke and/or fire.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0390-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-10-23 |
| Published | 2023-11-29 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Philips North America |
| Distribution | US |
Product
Achieva 1.5T Conversion
Reason
Potential component failure in the Gradient Coil could product smoke and/or fire.
Identifiers
| code_info | Product No. 781283 & 781346; UDI-DI: (01)00884838009806(21)39001, (01)00884838009806(21)39027, (01)00884838009806(21)39…Product No. 781283 & 781346; UDI-DI: (01)00884838009806(21)39001, (01)00884838009806(21)39027, (01)00884838009806(21)39028, (01)00884838009806(21)39030, (01)00884838009806(21)39032, (01)00884838009806(21)39039, (01)00884838009806(21)39053, (01)00884838009806(21)39059, (01)00884838009806(21)39061, (01)00884838009806(21)39062, (01)00884838009806(21)39064, (01)00884838009806(21)39065, (01)00884838009806(21)39066, (01)00884838009806(21)39067, (01)00884838009806(21)39072, (01)00884838009806(21)39073, (01)00884838009806(21)39074, (01)00884838009806(21)39075, (01)00884838009806(21)39078, (01)00884838009806(21)39080, (01)00884838009806(21)39081, (01)00884838009806(21)39082, (01)00884838009806(21)39083, (01)00884838009806(21)39084, (01)00884838009806(21)39086, (01)00884838009806(21)39088, (01)00884838009806(21)39090, (01)00884838009806(21)39091, (01)00884838009806(21)39093, (01)00884838009806(21)39094, (01)00884838009806(21)39095, (01)00884838009806(21)39097, (01)00884838009806(21)39098, (01)00 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0390-2024%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.