BROSELOW TAPE
Received Feb 10, 2026
Report MW5183651 · MDR key 24307578
Device
Generic name
Airway, Oropharyngeal, Anesthesiology
Manufacturer
Sunmed Group Holdings, Llc Dba AirlifePatient
NA · Unknown
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
(B)(6); PHONE: (B)(6) EMAIL: (B)(6). THANK YOU FOR THE NEWSLETTER ARTICLE REGARDING THE BROSELOW TAPE DOSING ERROR FROM AIRLIFE. WE DISCOVERED THAT WE HAVE THESE TAPES WITH THE DESCRIBED ERROR. I FOUND THAT THIS COMPANY ALSO HAD A RECALL IN MAY FOR THE REV. 2 HTTPS//WWW.FDA.GOV/MEDICAL-DEVICES/MEDICAL-DEVICE-RECALLS-AND-EARLY_ALERTS/BROSELOW-PEDITRIC-EMERGENCY-RAINBOW-TAPE-RECALL-AIRLIFE-REMOVES-CERTAIN-BROSELOW-PEDIATRIC (HTTPS://WWW.FDA.GOV/MEDICAL-DEVICES/MEDICAL-DEVICE/RECALLS-AND-EARLY-ALERTS/BROSELOW-PEDIATRIC-EMERGENCY-RAINBOW-TAPE-RECALL-AIRLIFE-REMOVES-CERTAIN-BROSELOW-PEDIATRIC). WE CHECKED OUR REV 3 IN WHICH THOSE ISSUES IN THE RECALL ARE RESOLVED, BUT THE FLUMAZENIL AND ROCURONIUM ERRORS ARE PRESENT. IT SEEMS LIKE TWO VERSIONS IN A ROW CONTAINED SIGNIFICANT ERRORS. ERROR OCCURRED; MEDICATION DID NOT REACH PT.