Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0031-2020 — TxRx 15Ch Knee Coil 3T QED part number:Q7000008 Siemens Model # 10185460

U.S. FDA — Device Enforcement · United States · 2019-08-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0031-2020
Date of alert
2019-08-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Quality Electrodynamics LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10185460
Reported risk: Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.