Product Wiki · Recalls · Health Canada — Medical Devices

Performance Series Sagittal Blade (2019-03-18) — recall 59247

Health Canada — Medical Devices · Canada · 2019-03-29 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
59247
Date of alert
2019-03-29
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: A total of three (3) complaints were found over the past 5 years (20-Feb-2014 to 20-Feb-2019). The complaint devices were found upon incoming inspection and were not used during a surgical procedure. During manufacture, packaging materials for a small portion of the lot may not have been properly positioned, resulting in a potential breach in sterility.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/performance-series-sagittal-bl

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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