Product Wiki · Recalls · Health Canada — Medical Devices

Devon Light Gloves and K-1920 Kits (2015-04-20) — recall 53181

Health Canada — Medical Devices · Canada · 2015-05-26 · Type I

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Agency
Health Canada — Medical Devices
Recall identifier
53181
Date of alert
2015-05-26
Country / jurisdiction
Canada
Risk level
Type I
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Covidien is voluntary recalling specific lots of the Devon light gloves and specific sterile kits. This recall is being conducted due to the risk that Devon light gloves of these lots could contain splits or holes that could result in an unintentional transfer of microorganisms by the clinician from the light handle into the patient wound.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/devon-light-gloves-and-k-1920-

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.

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.