TxRx 15CH Knee Coil 1 — Class II medical device recall Z-0032-2020
Terminated recall by Quality Electrodynamics LLC, reported 2019-10-09, distributed in NC. Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremit
| Recall number | Z-0032-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Quality Electrodynamics LLC, Mayfield Village, OH, United States |
| Recall initiated | 2019-08-20 |
| Classified | 2019-10-03 |
| Reported by FDA | 2019-10-09 |
| Terminated | 2020-05-26 |
| Distributed | NC |
| Countries outside the US | DE |
| Quantity | 3 units |
| Serial numbers | 1471, 1991, 2106 |
| Model numbers | 10185453, Q7000016 |
Product
TxRx 15CH Knee Coil 1.5T QED part number:Q7000016 Siemens Model # 10185453
Reason for recall
Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0032-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.