Two lots of Allerject emergency epinephrine devices have been recalled. If you have devices from these lots, return them immediately to your pharmacy for replacing.
Only blue (low dose) models are involved. Lot numbers can be found on the box or on the back of your individual unit.
Lot #285 7505
Lot #285 7508
Both lots show expiry dates of September 2016.
Canadian Newswire says:
As a result of a manufacturing defect with the needle, the device may not deliver the epinephrine needed for emergency treatment of serious allergic reactions (anaphylaxis), which can pose serious health risks to patients. Anaphylaxis may cause death. The dosage strength for this pre-filled, single-use auto injector is intended for use in children weighing between 15 kilograms and 30 kilograms. The affected lots were distributed starting June 1, 2015.
These are the only devices involved in a recall at this time.
Printer-friendly version