Nellcor™ Bedside SpO2 Patient Monitoring System
In plain language
This recall involves the Nellcor Bedside SpO2 Patient Monitoring System sold in Canada. It's being recalled because the device alarm may not be heard or recognized, which could delay treatment. Contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
Nellcor™ Bedside SpO2 Patient Monitoring System - Main Unit
Model: 10005941
Lot: All
Nellcor™ Bedside SpO2 Patient Monitoring System
Model: PM100N
Lot: All
Why this matters
Delay in treatment due to unrecognised alarm
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: All
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 10005941, PM100N
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?
Delay in treatment due to unrecognised alarm
What should consumers do?
Contact the manufacturer if you require 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. Delay in treatment due to unrecognised alarm
When was this product recalled?
This product was recalled on June 25, 2025.
Is the COVIDIEN LLC brand affected by this recall?
Yes, COVIDIEN LLC products are affected by this recall. This recall involves the Nellcor Bedside SpO2 Patient Monitoring System sold in Canada. It's being recalled because the device alarm may not be heard or recognized, which could delay treatment. Contact the manufacturer for more information.