Hydromorphone hydrochloride injection recall in Canada: Sterility risk
In plain language
This recall involves Hydromorphone hydrochloride injection USP sold in Canada. It's being recalled because product sterility may be compromised due to cracked vials. This could lead to serious health consequences. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check the lot number 67240DD.
- Return the product as instructed by Pfizer Canada Inc.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
Hydromorphone hydrochloride injection USP
Lot: 67240DD
Why this matters
Sterility risk
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: 67240DD
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?
Sterility risk
What should consumers do?
Stop using the product immediately. Check the lot number 67240DD. Return the product as instructed by Pfizer Canada Inc.
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. Sterility risk
When was this product recalled?
This product was recalled on January 31, 2018.