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Full Osseotite Implant — recall 48472

Health Canada — Medical Devices · Canada · 2012-11-26 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 48472
Date of alert: 2012-11-26
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 small number of implants from the above referenced lot number may contain a manufacturing condition where the depth of the implant's internal hex is too shallow. The condition, if present, may prevent the driver or abutment from fully engaging the implant.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/full-osseotite-implant

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Full Osseotite Implant — recall 48472

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