Product Wiki · Recalls · Health Canada — Medical Devices

CUSTOM TRILOGY STYLE ALLOFIT IT INSERTER (2015-11-24) — recall 54572

Health Canada — Medical Devices · Canada · 2016-01-14 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
54572
Date of alert
2016-01-14
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Zimmer Biomet is initiating a lot specific recall of the Trilogy style Allofit it inserters, part number 82-0174-140-00. Zimmer Biomet received two complaints for three devices which had bent and cracked at the weld which connects the Allofit it inserter handle to the Allofit it inserter tip. The affected devices were distributed between 25 June 2011 and 28 December 2012.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/custom-trilogy-style-allofit-i

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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