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
See all recalls from Bausch →Recalled Product
Emerade epinephrine auto-injectors, 0.3 mg (DIN 02458446) and 0.5 mg (DIN 02458454)
✅ What Should You Do?
- ⚠️ Stop using this product until you have checked the recall details below.
- Follow the instructions from the issuing agency (see below).
- 💰 Check if you are eligible for a refund or free replacement from the retailer or manufacturer.
- 📋 Report a product safety incident to Health Canada
Looking for a safe alternative?
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Hazard / Issue
Other
Issued by
Communications and Public Affairs Branch
⚠️ What You Should Do
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.
⚖️ Were You Affected?
If you were injured or suffered a loss due to this recalled product, you may have legal options.
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