Quality Electrodynamics recalls Siemens Knee and Extremity Coils with part number Q7000056 and model 10606828 due to potential ferrous material in pushbutton assembly. Affected units may pose safety risks.
Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
Quality Electrodynamics is recalling Siemens Knee and Extremity Coils with part number Q7000056 and model 10606828 because unintended ferrous material may be present in the pushbutton assembly. This could pose a safety risk if the material causes interference with medical equipment or other hazards.
The pushbutton assembly of the coil may contain unintended ferrous material, which could interfere with medical imaging equipment or cause other safety issues. This material might not be visible or detectable during normal use, making it a potential hazard.
Owners of Siemens Knee and Extremity Coils with part number Q7000056 and model 10606828 are affected. Patients using these coils for medical imaging may be at risk if the ferrous material causes interference.
Check for the part number Q7000056 and model number 10606828 on the coil. The serial numbers listed in the recall include a range of numbers starting with 1694 through 3318.
Look for the part number Q7000056 and model number 10606828 on the coil.
Unintended ferrous material may be present in the pushbutton assembly, which could interfere with medical imaging equipment or cause other safety issues.
Check for the part number Q7000056 and model number 10606828. Affected units have serial numbers starting with 1694 through 3318.
The recall does not specify a remedy, so contact Quality Electrodynamics for further instructions.
We’ve drafted a message you can send Quality Electrodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-0036-2020 — Quality Electrodynamics Quality Electrodynamics Hello, I own a Quality Electrodynamics that is covered by recall Z-0036-2020 from Quality Electrodynamics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
