Vecuronium Bromide Injection recall in Canada: labelling errors
In plain language
This recall involves US-labelled Vecuronium Bromide Injection sold in Canada. It's being recalled because of potential labelling and packaging differences that could lead to medication errors. Healthcare professionals should be aware of these differences to prevent serious harm to patients.
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
Vecuronium Bromide Injection (US-labelled) 10 mg in a fliptop vial (1 mg/mL when reconstituted to 10 mL)
Why this matters
Medication error due to labelling differences
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.
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?
Medication error due to labelling differences
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?
Yes, there may be a health risk. Medication error due to labelling differences
When was this product recalled?
This product was recalled on April 29, 2020.