BD Alaris™ modules recall in Canada: performance issues
In plain language
This recall involves BD Alaris™ EtCO2, PCA, Syringe, and Pump Modules sold in Canada. They are being recalled because of an increase in bent connector contacts which could cause the devices to be inoperable. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer for additional information.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
Alaris™ EtCO2 Module
Model: 8300
Lot: More than 10 numbers, contact manufacturer.
Alaris™ PCA Module
Model: 8120
Lot: More than 10 numbers, contact manufacturer.
BD Alaris™ Syringe Module
Model: 8110
Lot: More than 10 numbers, contact manufacturer.
BD Alaris™ Pump Module
Model: 8100
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Device performance issues
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: 8100, 8110, 8120, 8300
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?
Device performance issues
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?
Yes, there may be a health risk. Device performance issues
When was this product recalled?
This product was recalled on August 30, 2024.
Is the BD Alaris brand affected by this recall?
Yes, BD Alaris products are affected by this recall. This recall involves BD Alaris™ EtCO2, PCA, Syringe, and Pump Modules sold in Canada. They are being recalled because of an increase in bent connector contacts which could cause the devices to be inoperable. Healthcare professionals should contact the manufacturer for more information.