Medrad Veris MR Monitor units The system is intended to recall
Medrad Veris MR Monitor units The system is intended to monitor physiological parameters of patients within any healthcare environment. The user…
Why was Medrad Veris MR Monitor units The system is intended to recalled?
The main board, P/N 301641, installed in some Medrad Veris MR Monitor units may be faulty and could lead to unexpected shutdown of the system while in use, resulting in the loss of vital signs information from the monitor.
What should I do if I have this product?
Review the official FDA enforcement record for current 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?
P/N 301641, Catalog #s 3011992, 3011992W, 3011993, 3011993W, 3011994, 3011994W, 3011996, 3011996W, 3014268, 3014268W, with multiple serial numbers.
- Product
- Medrad Veris MR Monitor units The system is intended to monitor physiological parameters of patients within any healthcare environment. The user…
- Recalling firm
- Medrad Mr Inc
- Quantity
- 922 units
- Distribution
- Worldwide Distribution: US (nationwide) and Internationally to: Canada.
- Recall date
- January 29, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)