FDA Device recall Z-0031-2020
TxRx 15Ch Knee Coil 3T QED part number:Q7000008 Siemens Model # 10185460
- FDA Device
- Class II
- terminated
- Published 2019-10-09
On 2019-10-09 the FDA classified a Class II recall of TxRx 15Ch Knee Coil 3T QED part number:Q7000008 Siemens Model # 10185460 by Quality Electrodynamics, citing unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0031-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-08-20 |
| Published | 2019-10-09 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Quality Electrodynamics |
| Distribution | NC |
Product
TxRx 15Ch Knee Coil 3T QED part number:Q7000008 Siemens Model # 10185460
Reason
Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
Identifiers
| code_info | Serial # 1459 1460 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0031-2020%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.