Print version of this report
TGA Action ID RC-2026-RN-00120-1
Type of Product Medical Device
Product Name/Description Broselow Rainbow Tape (2025 Edition, 36-23446 Rev 3)

Product Codes: 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 three 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).

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

This action has been undertaken prior to notification to the TGA.

Update 02/03/2026: AirLife has identified an additional medication-related print error. The incorrect dosage information affects Mannitol.
Instructions for Customers/Users - Stop using the affected tapes and quarantine the affected product immediately.
- Return the affected product back to the supplier.
- This action was initiated prior to TGA notification.

This action has been finalised on 7/4/2026.
Action Commencement Date 13/02/2026
Responsible Entity Medical Devices Pty Ltd
Contact Information (02) 9743 3888 - Medical Devices