Mevatron M2/Primus Mid-Energy PRIMUS HI recall: Software Issue
Mevatron M2/Primus Mid-Energy PRIMUS HI
Why was Mevatron M2/Primus Mid-Energy PRIMUS HI recalled?
Software update
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?
Device Model# 1940035, 4504200
- Product
- Mevatron M2/Primus Mid-Energy PRIMUS HI
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 80 systems
- Distribution
- Distributed throughout the United States
- Recall date
- March 29, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)