Xvivo Organ Chamber recall in Canada: compromised sterile barrier
In plain language
This recall involves the Xvivo Organ Chamber sold in Canada. It's being recalled because the sterile barrier of the packaging may be compromised. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model and lot numbers.
- Contact the manufacturer for additional information.
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Affected products
Xvivo Organ Chamber
Model: 19020
Lot: 13801 To 13806
Why this matters
Compromised 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: 13801 To 13806
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 19020
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?
Compromised sterile barrier
What should consumers do?
Stop using the product immediately. Check model and lot numbers. 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?
Yes, there may be a health risk. Compromised sterile barrier
When was this product recalled?
This product was recalled on April 25, 2022.
Is the Xvivo Perfusion Ab brand affected by this recall?
Yes, Xvivo Perfusion Ab products are affected by this recall. This recall involves the Xvivo Organ Chamber sold in Canada. It's being recalled because the sterile barrier of the packaging may be compromised. Stop using the product and follow the return/repair steps in the official notice.