Product Wiki · Recalls · Health Canada — Medical Devices

Dermatome An Handpiece (2018-06-12) — recall 61067

Health Canada — Medical Devices · Canada · 2018-06-22 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
61067
Date of alert
2018-06-22
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Zimmer Biomet is conducting a medical device recall for specific serial numbers of Dermatome An. The affected devices could potentially have a loose control bar, which could compromise the ability to control the thickness of the graft. The affected devices could also potentially have a loose width plate that if undetected, could result in an imperfect, yet still usable graft.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/dermatome-handpiece-2018-06-12

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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