Product Wiki · Recalls · Health Canada — Medical Devices

ZIMMER PERIARTICULAR LOCKING PLATE (2016-01-04) — recall 54792

Health Canada — Medical Devices · Canada · 2016-01-22

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
54792
Date of alert
2016-01-22
Country / jurisdiction
Canada
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Zimmer Biomet is initiating a recall of non-sterile locking plate screws as it was found through a review of complaints that the product on the package label did not match what was inside the package. The label was for part number 00-2359-058-35 (a 58mm length screw) while the product inside the package was part number 00-2359-014-24 (a 14mm length screw).
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/zimmer-periarticular-locking-p

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.