Zimmer Hip and Shoulder Replacement Parts (2016-01-22) — recall 54896
Health Canada — Medical Devices · Canada · 2016-02-08 · 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 →
Archived by the issuing authority — kept for reference
Reported risk: In a follow-up correction, Zimmer Biomet is removing from the field a subset (from Zimmer GmbH) of highly polished implants that were packaged in a low density polyethylene (LDPE) bag with a potential to adhere to the implants. In September 2013, customers were asked to examine devices before use and return any showing signs of LDPE adhesion. At that time a new bag was introduced that resolves the issue and prevents the bag from adhering to the implants.
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.