Quality Electrodynamics recalls Siemens TxRx Knee 15 Coil 1.5T (QED part Q7000057) due to possible ferrous material in pushbutton assembly. Affected units have specific serial numbers. Contact for remedy.
Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
Quality Electrodynamics is recalling Siemens TxRx Knee 15 Coils with model number 10606829 that may contain unintended ferrous material in the pushbutton assembly. This could pose a risk during MRI scans if the material causes interference or injury.
The pushbutton assembly may contain unintended ferrous material, which could cause interference with MRI scans. This might lead to inaccurate imaging or potential injury if the material moves during scanning.
Owners of Siemens TxRx Knee 15 Coils with model number 10606829 and specific serial numbers listed in the recall. Patients undergoing MRI scans using these coils are at most risk.
Check for the Siemens model number 10606829 and specific serial numbers listed in the recall (1288 through 1179 and 1356). The product is sold by Quality Electrodynamics under part number Q7000057.
Verify the Siemens model number 10606829 and serial numbers listed in the recall (1288 through 1179 and 1356).
The recall indicates a possible presence of unintended ferrous material in the pushbutton assembly, which could cause interference with MRI scans. However, the risk is low and not immediately dangerous.
Check for the Siemens model number 10606829 and specific serial numbers listed in the recall (1288 through 1179 and 1356).
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-0037-2020 — Quality Electrodynamics Quality Electrodynamics Hello, I own a Quality Electrodynamics that is covered by recall Z-0037-2020 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.
