Product Wiki · Recalls · Health Canada — Medical Devices

Male External Catheter (2019-02-27) — recall 59053

Health Canada — Medical Devices · Canada · 2019-03-15 · Type III

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
59053
Date of alert
2019-03-15
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Teleflex Medical is voluntarily recalling the product referenced above as the shipper labels of the device contain a "sterile" symbol while in fact this is not a sterile product. The products are bulk packaged and do not contain individual level label.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/male-external-catheter-2019-02

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.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.