Abviser Intra-Abdominal Pressure Monitoring Kit (2018-06-21)
In plain language
This recall involves the Abviser Intra-Abdominal Pressure Monitoring Kit sold in Canada. It's being recalled because of a risk of pinhole breaches in the sterile barrier during shipment. 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 ConvaTec Inc. for instructions.
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Affected products
Abviser Intra-Abdominal Pressure Monitoring Kit
Model: ABV301
Lot: 161128, 170801
Why this matters
Risk of pinhole breach in sterile barrier
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: 161128, 170801
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: ABV301
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?
Risk of pinhole breach in sterile barrier
What should consumers do?
Stop using the product immediately. Check the lot and model numbers. Contact ConvaTec Inc. for 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. Risk of pinhole breach in sterile barrier
When was this product recalled?
This product was recalled on July 5, 2018.
Is the Abviser brand affected by this recall?
Yes, Abviser products are affected by this recall. This recall involves the Abviser Intra-Abdominal Pressure Monitoring Kit sold in Canada. It's being recalled because of a risk of pinhole breaches in the sterile barrier during shipment. Stop using the product and follow the return steps in the official notice.