Product Wiki · Recalls · Health Canada — Medical Devices

Broselow™/Hinkle Pediatric Emergency System — recall 81387

Health Canada — Medical Devices · Canada · 2025-12-19 · 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 →
Agency
Health Canada — Medical Devices
Recall identifier
81387
Date of alert
2025-12-19
Country / jurisdiction
Canada
Risk level
Type I
Risk type
recall
Product category
General hospital and personal use
Product type
Medical devices
Reported risk: AirLife™ has identified three medication-related errors in the content printed on the affected product version of the AirLife™ Broselow™ Rainbow Tape. Incorrect dosage of ketamine, flumazenil, and vecuronium is listed on the color zones of the Broselow™ tape which could potentially lead to an adverse event.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/broselowtmhinkle-pediatric-eme

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.