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

Recall Z-1569-2014 — Shimadzu Digital Radiography X-Ray System, Catalog No. DAR-8000f. This device is intended to be used for radiography in the hospital with X-ray devices.

U.S. FDA — Device Enforcement · United States · 2014-04-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1569-2014
Date of alert
2014-04-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Shimadzu Medical Systems
Product category
device
Product type
Devices
Reported risk: Shimadzu Corporation is recalling the Shimadzu Digital X-Ray System because they have received a report of a lost image under certain circumstances.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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