Product Wiki · Recalls · Health Canada — Medical Devices

Giraffe/Panda IRES Warmer — recall 64422

Health Canada — Medical Devices · Canada · 2022-08-02 · 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 →
Agency
Health Canada — Medical Devices
Recall identifier
64422
Date of alert
2022-08-02
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
General hospital and personal use
Product type
Medical devices
Reported risk: The field action FMI 32067/ and customer communication, plus enhanced panel design were launched in March 2019 and July 2020, respectively. However, GE Healthcare recently received one complaint of a patient fall related to the bedside panels not being latched as instructed. DYR 195 (FMI 32083) is to ensure continued awareness of the previously communicated safety instructions related to FMI 32067 to avoid the risk of patient falls. Recall start date: July 20, 2022
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/giraffepanda-ires-warmer

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.