Print version of this report
TGA Action ID RC-2026-RN-00152-1
Type of Product Medical Device
Product Name/Description Broselow Rainbow Tape

2025 Edition, 36-23446 Rev 3

Reference Numbers; 7700REA, 7700RE, 7730ALS, 7730IALS, AE4700, AE4800
ARTG Number
Action Type Recall
Action Level Hospital
Hazard Classification Class I
Reason for the Action There are multiple content discrepancies on the AirLife Broselow Rainbow Tape (2025 Edition, 36-23446 Rev 3). AirLife has identified four medication-related errors in the content printed on the affected version. The incorrectly printed medication dosages affect the information of Vecuronium, Flumazenil and Ketamine (IV/IO for pain/analgesia), and Mannitol.

No patient injuries or adverse events have been reported to date.

This action has been undertaken prior to notification to the TGA.
Instructions for Customers/Users Salient Training in Emergency Medicine International (STEMI) has advised customers to remove affected devices from clinical care and destroy them.

This action has been closed out on 18/03/2026
Action Commencement Date 27/02/2026
Responsible Entity Salient Training in Emergency Medicine International (STEMI)
Contact Information 0423 365 570 - STEMI