Product Wiki · Recalls · Health Canada — Medical Devices

Profile-II A (2014-10-20) — recall 52277

Health Canada — Medical Devices · Canada · 2014-11-04 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
52277
Date of alert
2014-11-04
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Health products
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: The recall arose out of one complaint received on September 22, 2014 which indicated that the control (CTRL) line for the oxycodone (OXY) test is not aligned with the marked ctrl position on the device top. When using lot 101, P/N 601681 Profile-II A 7-panel drugs of abuse screening devices.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/profile-ii-2014-10-20

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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.