Emerade injection; Device failure
CanadaEmerade injection; Device failure
Recalling Firm: Drugs and health products
Reason for Recall / Hazard
Product quality
Product Description & Identification
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.
Affected Products
Emerade Injection (0.3 mg / 0.3 mL and 0.5 mg / 0.5 mL)
Additional Source Details
| Field | Value |
|---|---|
| N I D | 73637 |
| U R L | https://recalls-rappels.canada.ca/en/alert-recall/emerade-injection-device-failure |
| Issue | Product quality |
| Title | Emerade injection; Device failure |
| Product | Emerade Injection (0.3 mg / 0.3 mL and 0.5 mg / 0.5 mL) |
| Archived | 0 |
| Category | Drugs |
| Last updated | 2023-05-08 |
| Organization | Drugs and health products |
| Recall class | Type I |
| 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. |
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Overview
- Recalling FirmDrugs and health products
- Risk LevelType I
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