Presource Procedure Packs recall in Canada: Device compatibility issue
In plain language
This recall involves Presource Procedure Packs sold in Canada. They are being recalled because of a device compatibility issue with a component. This recall is for healthcare facilities to quarantine and label affected inventory.
What to do
- Quarantine affected inventory.
- Affix the supplied warning label to discard the component.
- Return the reply form.
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Affected products
Presource Procedure Packs
Model: SAN30LPGBB, SBA30LBNHD, SBA30LBYCB
Lot: 656401, 795238, 718556, 713939, 711087, 631781, 696297, 786839, 715657
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: 656401, 795238, 718556, 713939, 711087, 631781, 696297, 786839, 715657
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: SAN30LPGBB, SBA30LBNHD, SBA30LBYCB
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 Presource Procedure Packs sold in Canada. They are being recalled because of a device compatibility issue with a component. This recall is for healthcare facilities to quarantine and label affected inventory.
What should consumers do?
Quarantine affected inventory. Affix the supplied warning label to discard the component. Return the reply form.
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 30, 2022.
Is the Cardinal Health brand affected by this recall?
Yes, Cardinal Health products are affected by this recall. This recall involves Presource Procedure Packs sold in Canada. They are being recalled because of a device compatibility issue with a component. This recall is for healthcare facilities to quarantine and label affected inventory.