Product Wiki · Recalls · Health Canada — Medical Devices

Reuter Bobbin Vent Tubes and T-Tubes (2016-12-28) — recall 56446

Health Canada — Medical Devices · Canada · 2017-01-18 · 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
56446
Date of alert
2017-01-18
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Boxes of 510-101 Lot 53226 and 500-101 Lot 53240 were packaged at the same time during final packaging. Final packaging consists of placing sealed sterile pouched tubes in boxes and labeling the boxes. Some of the final packed boxes had a mixture of these two tubes. All pouches were packaged and labeled correctly.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/reuter-bobbin-vent-tubes-and-t

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.