Monoject Blunt Cannula, Monoject Standard Hypodermic Needles (2019-04-28)
In plain language
This recall involves Monoject Blunt Cannula and Monoject Standard Hypodermic Needles sold in Canada. They are being recalled because a manufacturing defect could compromise the sterility, which may lead to infection. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check the lot and model numbers provided.
- Contact Cardinal Health for return instructions.
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Affected products
Monoject Blunt Cannula
Model: 8881202314, 8881202322, 8881202355, 8881202363, 8881202389
Lot: 902110, 902111, 903530, 905617, 905618, 905619, 905620, 905659, 905660, 906343, 907004, 907005, 907734
Monoject Standard Hypodermic Needles
Model: 8881200011, 8881200029, 8881200037, 8881200045, 8881200078, 8881200508
Lot: 904212, 904218, 904901, 904918, 904956, 905612, 905613, 906329, 907002, 907007
Why this matters
Infection risk due to compromised sterility
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: 902110, 902111, 903530, 905617, 905618, 905619, 905620, 905659, 905660, 906343, 907004, 907005, 907734, 904212, 904218, 904901, 904918, 904956, 905612, 905613, 906329, 907002, 907007
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 8881200011, 8881200029, 8881200037, 8881200045, 8881200078, 8881200508, 8881202314, 8881202322, 8881202355, 8881202363, 8881202389
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?
Infection risk due to compromised sterility
What should consumers do?
Stop using the product immediately. Check the lot and model numbers provided. Contact Cardinal Health for return instructions.
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. Infection risk due to compromised sterility
When was this product recalled?
This product was recalled on May 10, 2019.
Is the Monoject brand affected by this recall?
Yes, Monoject products are affected by this recall. This recall involves Monoject Blunt Cannula and Monoject Standard Hypodermic Needles sold in Canada. They are being recalled because a manufacturing defect could compromise the sterility, which may lead to infection. Stop using the product and follow the return steps in the official notice.