INFUSION SET - BURETTE SET YS MC (2021-08-06) — recall 62776
Health Canada — Medical Devices · Canada · 2021-08-19 · Type II
🏛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 →
Reported risk: Recall is being initiated as based on customer feedback, BD has identified potential issues with the valve of the Needle-free Connector for a number of impacted products codes/lots resulting in difficulty to flush, flow issues, and partial or total occlusions on the Extension Sets with SmartSite⢠and Standalone SmartSite⢠connectors.
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.