Casirivimab and Imdevimab recall in Canada: English-only labels
In plain language
This recall involves Casirivimab and Imdevimab concentrate for solution for infusion sold in Canada. It's being recalled because the packaging has English-only labels, missing Canadian-specific information and French text. Healthcare professionals should use the Canadian Product Monograph for complete product information.
What to do
- Stop using the product immediately.
- Check model/serial numbers if provided.
- Return, repair, or dispose of it as instructed.
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Affected products
Casirivimab and Imdevimab concentrate for solution for infusion (20 mL vial size)
Model: DIN 02516705
Casirivimab and Imdevimab concentrate for solution for infusion (6 mL vial size)
Model: DIN 02516691
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 model number
Model numbers are typically on the product label or packaging.
Affected models: DIN 02516691, DIN 02516705
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?
This recall involves Casirivimab and Imdevimab concentrate for solution for infusion sold in Canada. It's being recalled because the packaging has English-only labels, missing Canadian-specific information and French text. Healthcare professionals should use the Canadian Product Monograph for complete product information.
What should consumers do?
Stop using the product immediately. Check model/serial numbers if provided. Return, repair, or dispose of it as instructed.
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?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on July 30, 2021.