Siemens Mobilett Mira mobile x-ray system Product recall
Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray system
Why was Siemens Mobilett Mira mobile x-ray system Product recalled?
During regular product monitoring, firm became aware of a potential issue with the Mobilett Mira system, (serial numbers 1034, 1038, 1041, 1042, 1043, 1050, 1053, and 1054. During normal clinical operation the center screw on the driving wheel may become loose resulting in system immobilization. There is no risk of the system tipping over or collapsing on the floor, however the system may tilt t
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 - serial numbers 1034, 1038, 1041, 1042, 1043, 1050, 1053, and 1054
- Product
- Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray system
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 9
- Distribution
- US Nationwide Distribution including the states of: GA, IA, KS, NC and TX.
- Recall date
- September 19, 2012
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)