BD Alaris Infusion Devices recall in Canada: Device compatibility issue
In plain language
This recall involves BD Alaris Infusion Devices sold in Canada. It's being recalled because certain syringes have not been validated for use with these devices, which may impact their function. This recall is for healthcare professionals. Contact the manufacturer for more information.
What to do
- Contact the manufacturer for additional information.
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Affected products
BD Alaris PC Unit
Model: 8015
Lot: More than 10 numbers, contact manufacturer.
BD Alaris Syringe Module
Model: 8110
Lot: More than 10 numbers, contact manufacturer.
Alaris Patient-Controlled Analgesia (PCA) Module
Model: 8120
Lot: More than 10 numbers, contact manufacturer.
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: 8015, 8110, 8120
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 BD Alaris Infusion Devices sold in Canada. It's being recalled because certain syringes have not been validated for use with these devices, which may impact their function. This recall is for healthcare professionals. Contact the manufacturer for more information.
What should consumers do?
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?
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 October 30, 2023.
Is the Carefusion 303, Inc. brand affected by this recall?
Yes, Carefusion 303, Inc. products are affected by this recall. This recall involves BD Alaris Infusion Devices sold in Canada. It's being recalled because certain syringes have not been validated for use with these devices, which may impact their function. This recall is for healthcare professionals. Contact the manufacturer for more information.