AUSTRALIAN PRODUCT RECALL

EPIPEN 300 microgram (µg) Adrenaline Injection Syringe Auto-Injector (AUST R 42978)

Published 22 March 2017

Product

The following batches of EpiPen® 300 microgram (µg) Adrenaline Injection Syringe Auto-Injectors (AUST R 42978) used for the treatment of allergic emergencies (anaphylaxis)): Batch number 5FA665 Expiry Apr 17 Batch number 5FA6651 Expiry Apr 17 Batch number 5FA6652 Expiry Apr 17 Batch number 5FA6653 Expiry Apr 17

Why it was recalled

There is a potential that these devices may contain a defective part that may result in the device failing to activate or requiring increased force to activate.

Hazard

The failure of the auto-injector to activate may result in patients not receiving the required dose of adrenaline, causing the worsening of symptoms of anaphylaxis or anaphylactic reactions, which could be life threatening.

Read the official notice ↗

Source: Product Safety Australia. RecallMatch AU provides a screening summary and is independent of the ACCC.