Product Wiki · Recalls · Health Canada — Medical Devices

Kodak 2100 and 2200 Intraoral X-Ray System (2014-03-03) — recall 51525

Health Canada — Medical Devices · Canada · 2014-04-04 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
51525
Date of alert
2014-04-04
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: A potential problem which could result in an early failure of the scissor arm to bracket connection. The failure can be identified by observing the physical condition of the scissor arm bracket. The plastic covers around the bracket typically show signs of fatigue before the bracket actually breaks. This can be an early indicator of a potential problem.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/kodak-2100-and-2200-intraoral-

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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