Product Wiki · Recalls · Health Canada — Medical Devices

Cardiosave Hybrid And Rescue Intra-Aortic Balloon Pump — recall 56461

Health Canada — Medical Devices · Canada · 2017-01-25 · 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 →
Agency
Health Canada — Medical Devices
Recall identifier
56461
Date of alert
2017-01-25
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: If the lithium-ion battery is accidently dropped, the impact may cause the battery to vent. In addition to the risks contained in the warnings section of the operator/user instructions, battery venting has the pot
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/cardiosave-hybrid-and-rescue-i

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.