Product Wiki · Recalls · Health Canada — Medical Devices

Non Absorbable Silky II Polydek Suture (2014-03-24) — recall 52883

Health Canada — Medical Devices · Canada · 2014-11-21 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
52883
Date of alert
2014-11-21
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: Teleflex is conducting a voluntary recall for certain lots of Teleflex sutures because they did not meet minimum needle attachment strength requirements. If affected product is used, the needle may become detached from the suture during use.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/non-absorbable-silky-ii-polyde

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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