Product Wiki · Recalls · Health Canada — Medical Devices

DLP Elongated One Piece and Select 3D Arterial Cannula (2014-01-30) — recall 50755

Health Canada — Medical Devices · Canada · 2014-03-18 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
50755
Date of alert
2014-03-18
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: A field corrective action is being initiated to recall all Select 3D and DLP Elongated One Piece Arterial Cannula due to an increase in reports of the cannula body splitting near the suture collar. Potential harm from the cannula body split near the suture collar may include inadequate blood flow, resulting in ischemia or inadequate perfusion
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/dlp-elongated-one-piece-and-se

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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.