Cardinal Health Cardiovascular, Bypass and Hepatobiliary Packs — recall 75220
Health Canada — Medical Devices · Canada · 2024-03-12 · Type I
🏛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 →
Cardiovascular - General hospital and personal use
Product type
Medical devices
Reported risk: The recent expansion to medical device recall from Medtronic/Covidien concerning various sutures found in some Cardinal Health Presource® kits. Specific lots of these sutures were sterilized with gamma doses that exceed the range approved or were exposed to more than the approved number of ethylene oxide (EO) sterilization cycles. Recall Start Date: February 29, 2024
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.