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Emerade epinephrine auto-injectors, 0.3 mg (DIN 02458446) and 0.5 mg (DIN 02458454)
Official notice
5 May 2023
Last checked
5 May 2023
An official Health Canada notice concerns Emerade epinephrine auto-injectors, 0.3 mg (DIN 02458446) and 0.5 mg (DIN 02458454). Bausch Health, Canada Inc. Recalls all lots of Emerade epinephrine auto-injectors (0.3 mg and 0.5 mg strengths) due to possible device failure Published 2023-05-05.
What to do now
Consult your pharmacist to ensure you understand how to properly use the replacement auto-injector. In the event a life-threatening allergic reaction (anaphylaxis) occurs before you can obtain a replacement auto-injector, use your Emerade device and then seek emergency medical attention. Speak with your healthcare professional if you are concerned about your health. Contact Bausch Health, Canada Inc. By calling 1-800-361-4261, or emailing canada. Customerservice@bauschhealth. Com , if you have questions about the recall. Report any health product-related side effects or complaints to Health Canada.
Recall number
73621
Official notice
2023-05-05
The hazard
The hazard
Bausch Health, Canada Inc. Recalls all lots of Emerade epinephrine auto-injectors (0.3 mg and 0.5 mg strengths) due to possible device failure
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
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Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Emerade Epinephrine Auto-injectors 0.3 MG And 0.5 MG.
Source & status
Source & status
Source
Tier
Category
App estimate
Recall details
Recall details
Recall number
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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