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

Recall Z-1040-2015 — MobileDiagnost wDR motorized portable diagnostic X-ray systems.

U.S. FDA — Device Enforcement · Spain · 2014-08-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1040-2015
Date of alert
2014-08-06
Country / jurisdiction
Spain
Risk level
Class II
Risk type
recall
Brand
Sedecal S.A.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
12000166
Reported risk: Reports of unexpected movement.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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