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

Recall Z-0126-2014 — Carestream DRX-Revolution Mobile X-ray System. Produces radiographic images.

U.S. FDA — Device Enforcement · United States · 2013-06-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0126-2014
Date of alert
2013-06-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Carestream Health, Inc.
Product category
device
Product type
Devices
Reported risk: Carestream Health Inc. is recalling the power plug on their DRX-Revolution Mobile X-Ray System due to the item generating sparks and becoming warm to touch.
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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