inforMED
InjuryOKI

BROSELOW PEDIATRIC EMERGENCY REFERENCE TAPE

Received Nov 17, 2025 · Event occurred Nov 12, 2025

Report MW5178930 · MDR key 23568571

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Product code (OKI)
Manufacturer (Sunmed Group Holdings, Llc Dba Airlife)
Model (36-23446 REV3)

Device

Generic name

Emergency Response Safety Kit

Model number

36-23446 REV3

Product problems

  • Inaccurate Information

Patient

NA · Unknown

  • No Clinical Signs, Symptoms or Conditions
  • No Clinical Signs, Symptoms or Conditions

Narrative

Description of Event or Problem

DURING A REVIEW OF THE 2025 VERSION 3 BROSELOW TAPE FROM AIRLIFE MANUFACTURING / ARMSTRONG MEDICAL, IT WAS FOUND THAT THE DOSING CARD REFERENCE CONTAINS INCORRECT INFORMATION FOR VECURONIUM AND FLUMAZENIL. UNDER "PRE-RIS/RSA NEUROMUSCULAR BLOCKERS" VECURONIUM IV/IO IS LISTED WITH A DOSE OF 0.1MG/ML. THIS SHOULD READ 0.1MG/KG. THE SECOND ERROR CONCERNS FLUMAZENIL IV/IO UNDER THE "TOXICOLOGY" SECTION! WHICH LISTS THE DOSE AS 0.1MG/KG, BUT THE DOSE SHOULD BE 0.01MG/KG. NO ERROR HAS REACHED A PATIENT AT THIS TIME, BUT ALL LOCAL USERS HAVE BEEN MADE AWARE OF THIS POTENTIAL ERROR. THE ISSUE HAS ALSO BEEN SENT TO AIRLIFE MEDICAL WITH NO RESPONSE.