Quality Electrodynamics recalls Siemens 10185460 knee coils due to possible ferrous material in pushbutton assembly. Affected units have QED part number Q7000008 and serial numbers 1459-1460. No remedy specified in recall notice.
Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
Quality Electrodynamics is recalling Siemens 10185460 knee coils with QED part number Q7000008 and serial numbers 1459-1460 because unintended ferrous material may be present in the pushbutton assembly. This could pose a risk if the material becomes dislodged during use, though the recall does not specify a remedy.
The pushbutton assembly in these knee coils may contain unintended ferrous material. If this material becomes dislodged during use, it could potentially interfere with MRI scans or cause injury. However, the recall does not specify how this material might become dislodged or the exact risk level.
Owners of Siemens 10185460 knee coils with QED part number Q7000008 and serial numbers 1459-1460 are affected. Patients using these coils for MRI scans are most at risk if the ferrous material becomes dislodged.
Check for the QED part number Q7000008 and Siemens model number 10185460 on the coil. Serial numbers 1459 and 1460 are also associated with this recall.
Verify the QED part number Q7000008, Siemens model number 10185460, and serial numbers 1459-1460 on the coil.
The recall notice does not specify any remedy for this issue.
The recall does not provide specific action steps; you should check the product details to confirm if it is affected.
Look for the QED part number Q7000008, Siemens model number 10185460, and serial numbers 1459-1460 on the coil.
We’ve drafted a message you can send Quality Electrodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-0031-2020 — Quality Electrodynamics Quality Electrodynamics Hello, I own a Quality Electrodynamics that is covered by recall Z-0031-2020 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.
