IntelliVue MX40 Patient Monitor recall
IntelliVue MX40 Patient Monitor, Product number 857146, Service Numbers All: 453564711531 and 453564711541 - Product Usage: Used primarily as a…
Why was IntelliVue MX40 Patient Monitor recalled?
The MX40 may experience increased power consumption and may have a lack of visual and/or audible notifications while in a Low Battery State .
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
All revision B.X versions are affected.
- Product
- IntelliVue MX40 Patient Monitor, Product number 857146, Service Numbers All: 453564711531 and 453564711541 - Product Usage: Used primarily as a…
- Recalling firm
- Philips North America, LLC
- Distribution
- Worldwide distribution - US Nationwide and to 71 countries.
- Recall date
- June 12, 2019
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)