Abbott Vascular Indeflator Device recall in Canada: Quality issue
In plain language
This recall involves Indeflator Devices from Abbott Vascular sold in Canada. It's being recalled because some devices may have leaks or loose connections. This could lead to air entering the device, which may cause an air embolism, thrombosis, or foreign body in the patient. Contact the manufacturer if you require additional information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Indeflator Plus 30 Inflation Device
Model: 1000183, 1000185
Lot: More than 10 numbers, contact manufacturer.
20/30 Priority Pack Accessory Kit With Copilot
Model: 1003327
Lot: More than 10 numbers, contact manufacturer.
20/30 Indeflator Inflation Device
Model: 1000184, 1000186, 1000186-115
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Air embolism, thrombosis, or foreign body in patient
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: More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 1000183, 1000184, 1000185, 1000186, 1000186-115, 1003327
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?
Air embolism, thrombosis, or foreign body in patient
What should consumers do?
Contact the manufacturer if you require 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?
Yes, there may be a health risk. Air embolism, thrombosis, or foreign body in patient
When was this product recalled?
This product was recalled on March 28, 2022.
Is the Abbott Vascular brand affected by this recall?
Yes, Abbott Vascular products are affected by this recall. This recall involves Indeflator Devices from Abbott Vascular sold in Canada. It's being recalled because some devices may have leaks or loose connections. This could lead to air entering the device, which may cause an air embolism, thrombosis, or foreign body in the patient. Contact the manufacturer if you require additional information.