Minicap Disconnect Cap recall in Canada: packaging defect
In plain language
This recall involves Minicap Disconnect Caps with Povidone-Iodine sold in Canada. They are being recalled because the foil pouches may have incorrect or weak seals. Stop using the product and contact the manufacturer for more information.
What to do
- Stop using the product immediately.
- Contact the manufacturer for additional information.
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Affected products
Minicap Disconnect Cap With Povidone-Iodine
Model: 5C4466P
Lot: More than 10 numbers, contact manufacturer.
Date codes: expire on or before May 31, 2024
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 date code
Date codes are usually printed near the best-before date or on the packaging seam.
Affected date codes: expire on or before May 31, 2024
- 3
Check the lot number
Lot numbers identify specific production batches.
Affected lots: More than 10 numbers, contact manufacturer.
- 4
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 5C4466P
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 Minicap Disconnect Caps with Povidone-Iodine sold in Canada. They are being recalled because the foil pouches may have incorrect or weak seals. Stop using the product and contact the manufacturer for more information.
What should consumers do?
Stop using the product immediately. Contact the manufacturer for additional information.
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 May 10, 2023.
Is the Baxter Healthcare Corporation brand affected by this recall?
Yes, Baxter Healthcare Corporation products are affected by this recall. This recall involves Minicap Disconnect Caps with Povidone-Iodine sold in Canada. They are being recalled because the foil pouches may have incorrect or weak seals. Stop using the product and contact the manufacturer for more information.