FDA Device recall Z-0036-2020
TxRx Knee 15 Coil 1.5T QED part number: Q7000056 Siemens Model # 10606828
- FDA Device
- Class II
- terminated
- Published 2019-10-09
On 2019-10-09 the FDA classified a Class II recall of TxRx Knee 15 Coil 1.5T QED part number: Q7000056 Siemens Model # 10606828 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-0036-2020 |
| 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 Knee 15 Coil 1.5T QED part number: Q7000056 Siemens Model # 10606828
Reason
Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
Identifiers
| code_info | Serial # 1694 1841 1887 1933 1998 3195 3291 3292 3293 3294 3298 3299 3300 3301 3302 3303 3304 3305 3…Serial # 1694 1841 1887 1933 1998 3195 3291 3292 3293 3294 3298 3299 3300 3301 3302 3303 3304 3305 3306 3307 3308 3309 3310 3311 3312 3313 3314 3315 3316 3317 3318 ¿1137 ¿1361 ¿1378 ¿1628 ¿2447 |
|---|
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-0036-2020%22
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