Emerade injection recall in Canada: Device failure
In plain language
This recall involves Emerade 0.3 mg and 0.5 mg auto-injectors sold in Canada. They are being recalled because the devices may malfunction. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Return your Emerade auto-injector to your pharmacy for a suitable replacement as soon as possible.
- Do not return or dispose of your Emerade auto-injector until a replacement is obtained.
- If a life-threatening allergic reaction occurs before you get a replacement, use your recalled Emerade and then seek emergency medical attention.
- Consult your pharmacist to ensure you understand how to properly use the replacement auto-injector.
- Contact Bausch Health, Canada Inc. at 1-800-361-4261 or canada.customerservice@bauschhealth.com if you have questions.
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Affected products
Emerade 0.3 mg / 0.3 mL injection
Lot: Y0225B2A, Z0076B1A, Z0034B2C, Z0198B3A, Z0198B3B
Emerade 0.5 mg / 0.5 mL injection
Lot: Y0225C1A, Z0034C1A, Z0076C2A, Z0088C3A, Z0153C2A, Z0236C1C, Z0088C3B, Z0128C1B, Z0153C2B
Why this matters
Device failure
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: Y0225B2A, Z0076B1A, Z0034B2C, Z0198B3A, Z0198B3B, Y0225C1A, Z0034C1A, Z0076C2A, Z0088C3A, Z0153C2A, Z0236C1C, Z0088C3B, Z0128C1B, Z0153C2B
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Device failure
What should consumers do?
Return your Emerade auto-injector to your pharmacy for a suitable replacement as soon as possible. Do not return or dispose of your Emerade auto-injector until a replacement is obtained. If a life-threatening allergic reaction occurs before you get a replacement, use your recalled Emerade and then seek emergency medical attention. Consult your pharmacist to ensure you understand how to properly use the replacement auto-injector. Contact Bausch Health, Canada Inc. at 1-800-361-4261 or canada.customerservice@bauschhealth.com if you have questions.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Device failure
When was this product recalled?
This product was recalled on May 8, 2023.
Is the Emerade brand affected by this recall?
Yes, Emerade products are affected by this recall. This recall involves Emerade 0.3 mg and 0.5 mg auto-injectors sold in Canada. They are being recalled because the devices may malfunction. Stop using the product and follow the return/repair steps in the official notice.