Product Wiki · Recalls · Health Canada — Medical Devices

Nutriline, Catheter With Stylet And Microflash — recall 57367

Health Canada — Medical Devices · Canada · 2017-08-15 · 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
57367
Date of alert
2017-08-15
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: Two Vygon Nutriline kits are being recalled because it was found that they were packaged with an incorrect version of the microflash introducer. The version packaged in the affected product is a CE-marked version that is not yet cleared in the us or licensed in Canada. The change of introducer insider the Nutriline kits was made in error, as the un-licensed introducer was not approved to be in the Nutriline kits.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/nutriline-catheter-stylet-and-

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.