cobas p501 post-analytical units (2019-04-07) — recall 59367
Health Canada — Medical Devices · Canada · 2019-04-18 · 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: The tray input flap on the cobas p 501 and cobas p 701 post-analytical units has the potential to become unsecured from the instrument. The tray input flap screws can become loose on the cobas p 501 or p 701 post-analytical units resulting in the potential detachment from the instrument.
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.