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Procotyl and Profemur Products — recall 48305

Health Canada — Medical Devices · Canada · 2012-10-01 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 48305
Date of alert: 2012-10-01
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: Wright Medical Technology Inc. has determined there may be an inaccuracy on the labelled shelf life on all products packaged at the Toulon Facility.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/procotyl-and-profemur-products

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Procotyl and Profemur Products — recall 48305

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