Product Wiki · Recalls · Health Canada — Medical Devices

Knee Nozzle (2014-01-23) — recall 51341

Health Canada — Medical Devices · Canada · 2014-04-04 · 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
51341
Date of alert
2014-04-04
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: Following an investigation of a Canadian complaint alleging that the device was improperly assembled, Biomet France determined that devices from lot numbers 0000582617 and 0000568253 were indeed out of specification with regard to assembly. It was found that the knee nozzle was unable to thread onto Optipac tube for cement extraction using the gun.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/knee-nozzle-2014-01-23

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.