BD infusion sets recall in Canada: Sterilization concerns
In plain language
This recall involves various BD infusion sets, components, and extension sets sold in Canada. They are being recalled because a third-party sterilization facility may have falsified sterilization records. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Contact BD for more information.
- Follow the instructions provided by BD regarding affected products.
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Affected products
ALARIS SMARTSITE NEEDLE-FREE MULTI-WAY CONNECTING SET
Model: 2305E, 2306E
Lot: More than 10 numbers, contact manufacturer.
ALARIS INFUSION SET. VENTED
Model: 388000, 388002
Lot: More than 10 numbers, contact manufacturer.
SECONDARY SET COMPONENTS AND EXTENSION SETS
Model: 72951NE, G30402M, G40020B
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Potential infection risk due to improper sterilization
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: 2305E, 2306E, 388000, 388002, 72951NE, G30402M, G40020B
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?
Potential infection risk due to improper sterilization
What should consumers do?
Stop using the product immediately. Contact BD for more information. Follow the instructions provided by BD regarding affected products.
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. Potential infection risk due to improper sterilization
When was this product recalled?
This product was recalled on March 23, 2021.
Is the BD brand affected by this recall?
Yes, BD products are affected by this recall. This recall involves various BD infusion sets, components, and extension sets sold in Canada. They are being recalled because a third-party sterilization facility may have falsified sterilization records. Stop using the product and follow the return steps in the official notice.