Monoject Standard Hypodermic Needles recall in Canada: Puncture risk
In plain language
This recall involves Monoject Standard Hypodermic Needles sold in Canada. They are being recalled because the needle may detach from the cartridge, which could lead to a needle stick or puncture. 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.
- Contact Cardinal Health 200, LLC for return instructions.
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Affected products
Monoject Standard Hypodermic Needles
Model: 8881250248
Lot: 11144
Why this matters
Puncture risk from needle stick
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: 11144
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 8881250248
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?
Puncture risk from needle stick
What should consumers do?
Stop using the product immediately. Check the lot and model numbers. Contact Cardinal Health 200, LLC 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. Puncture risk from needle stick
When was this product recalled?
This product was recalled on October 23, 2020.
Is the Monoject brand affected by this recall?
Yes, Monoject products are affected by this recall. This recall involves Monoject Standard Hypodermic Needles sold in Canada. They are being recalled because the needle may detach from the cartridge, which could lead to a needle stick or puncture. Stop using the product and follow the return steps in the official notice.