Ambu Vivasight 2 Dlt Kit recall in Canada: Performance issue
In plain language
This recall involves the Ambu Vivasight 2 Dlt Kit sold in Canada. It's being recalled because of performance issues, specifically potential cuff leaks or ruptures. Healthcare professionals should confirm receipt of the field safety notice and destroy any remaining units in inventory.
What to do
- Confirm receipt of the field safety notice.
- Destroy any remaining units in inventory.
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Affected products
Ambu Vivasight 2 Dlt Kit
Model: 412351000, 412371000, 412391000, 412411000
Lot: All lots
Why this matters
Performance issue
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: All lots
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 412351000, 412371000, 412391000, 412411000
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?
Performance issue
What should consumers do?
Confirm receipt of the field safety notice. Destroy any remaining units in inventory.
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. Performance issue
When was this product recalled?
This product was recalled on June 20, 2022.
Is the Ambu A/S brand affected by this recall?
Yes, Ambu A/S products are affected by this recall. This recall involves the Ambu Vivasight 2 Dlt Kit sold in Canada. It's being recalled because of performance issues, specifically potential cuff leaks or ruptures. Healthcare professionals should confirm receipt of the field safety notice and destroy any remaining units in inventory.