BROSELOW RAINBOW TAPE
Received Jan 21, 2026 · Event occurred Nov 12, 2025
Report MW5182596 · MDR key 24134489
Device
Generic name
Emergency Response Safety Kit
Manufacturer
Sunmed Group Holdings, Llc Dba AirlifeModel number
REVISION 3, 36-23446Patient
NA · Unknown
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
THE 2025 BROSELOW TAPE WAS DISCOVERED TO HAVE ERRORS IN THE MEDICATION DOSES, SOME OF THEM SIGNIFICANT WITH POTENTIAL TO CAUSE HARM OR DEATH TO A PATIENT. SPECIFICALLY, -VECURONIUM: IN THE CALCULATION BASIS "RED TO HEAD" REFERENCE SECTION, THE DOSAGE IS SHOWN AS 0.1 MG/ML (CONCENTRATION) INSTEAD OF THE CORRECT 0.1 MG/KG (WEIGHT-BASED DOSE). -FLUMAZENIL: IN THE CALCULATION BASIS "RED TO HEAD" SECTION, THE DOSAGE IS SHOWN AS 0.1 MG/KG INSTEAD OF THE CORRECT 0.01 MG/KG. THE COLOR-CODED SECTIONS OF THE TAPE LIST THE CORRECT FLUMAZENIL DOSE, BUT THE REFERENCE TABLE IS INCORRECT AND REPRESENTS A 10-FOLD OVERDOSE. -KETAMINE (IV/IO FOR PAIN/ANALGESIA): THE TAPE LISTS IV/IO KETAMINE FOR PAIN/ANALGESIA AS 1 MG/KG, WHEREAS THE APPROPRIATE PEDIATRIC ANALGESIC (SUB-DISSOCIATIVE) DOSE IS 0.1 MG/KG. THIS REPRESENTS A 10-FOLD OVERDOSE AND MAY RESULT IN A DISSOCIATIVE SEDATION DOSE BEING ADMINISTERED WHEN ONLY ANALGESIA WAS INTENDED.