BD Phoenix System recall in Canada: inaccurate test results
In plain language
This recall involves BD Phoenix System NMIC 1 and NMIC 93 medical devices sold in Canada. They are being recalled because they may give inaccurate test results for Colistin-resistant bacteria. Healthcare professionals should stop using the affected products and follow the return steps in the official notice.
What to do
- Stop using the affected BD Phoenix System devices immediately.
- Check model numbers 448063, 448764, and 448788.
- Contact Becton Dickinson and Company for instructions on return or disposal.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
BD PHOENIX SYSTEM - NMIC 1
Model: 448063
Lot: 7095829, 7276978
BD PHOENIX NMIC-93
Model: 448764, 448788
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Inaccurate test results
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: 7095829, 7276978, More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 448063, 448764, 448788
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?
Inaccurate test results
What should consumers do?
Stop using the affected BD Phoenix System devices immediately. Check model numbers 448063, 448764, and 448788. Contact Becton Dickinson and Company for instructions on return or disposal.
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. Inaccurate test results
When was this product recalled?
This product was recalled on February 1, 2018.
Is the BD Phoenix System brand affected by this recall?
Yes, BD Phoenix System products are affected by this recall. This recall involves BD Phoenix System NMIC 1 and NMIC 93 medical devices sold in Canada. They are being recalled because they may give inaccurate test results for Colistin-resistant bacteria. Healthcare professionals should stop using the affected products and follow the return steps in the official notice.