Class II — Quality Electrodynamics LLC
| Recalling firm | Quality Electrodynamics |
|---|---|
| Registered facility | QUALITY ELECTRODYNAMICS (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils. |
| Product | TxRx Knee 15 Coil 1.5T QED part number: Q7000056 Siemens Model # 10606828 |
| Quantity | 36 units |
| Distribution | Worldwide distribution - US in the states: NC OUS: Germany |
| Initiated | 2019-08-20 |
| Classified | 2019-10-03 |
| Terminated | 2020-05-26 |
| Recall number | Z-0036-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Quality Electrodynamics LLC (Z-0036-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/83775/
Alerts for Quality Electrodynamics
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.