BD Alaris PCU recall in Canada: performance issue
In plain language
This recall involves the BD Alaris PCU, a medical device used in healthcare settings. It's being recalled because bent contacts on connectors could cause the device to be inoperable. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
- Check model number 8015.
- Note that this recall is for healthcare professionals.
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Affected products
BD Alaris PCU
Model: 8015
Lot: More than 10 numbers, contact manufacturer.
Date codes: manufactured between Jan 01, 2023 and June 06, 2024
Why this matters
Performance issue
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 date code
Date codes are usually printed near the best-before date or on the packaging seam.
Affected date codes: manufactured between Jan 01, 2023 and June 06, 2024
- 3
Check the lot number
Lot numbers identify specific production batches.
Affected lots: More than 10 numbers, contact manufacturer.
- 4
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 8015
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?
Performance issue
What should consumers do?
Contact the manufacturer if you require additional information. Check model number 8015. Note that this recall is for healthcare professionals.
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. Performance issue
When was this product recalled?
This product was recalled on September 11, 2024.
Is the Carefusion 303, Inc. brand affected by this recall?
Yes, Carefusion 303, Inc. products are affected by this recall. This recall involves the BD Alaris PCU, a medical device used in healthcare settings. It's being recalled because bent contacts on connectors could cause the device to be inoperable. Healthcare professionals should contact the manufacturer for more information.