Siemens Mobilette Mira recall
Siemens Mobilette Mira, intended use as Mobile x-ray system.
Why was Siemens Mobilette Mira recalled?
There is a risk of lost images during examination.
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?
Model Number 10273100
- Product
- Siemens Mobilette Mira, intended use as Mobile x-ray system.
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 21
- Distribution
- Nationwide distribution: USA including states of: GA, ID, IL, IA, NE, NC, OH, SD, TX, and WI.
- Recall date
- December 12, 2012
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)