Mobilett Mira wireless recall
Mobilett Mira wireless (VA20) mobile x-ray system(s)
Why was Mobilett Mira wireless recalled?
Due to the incorrect mounting of the buzzer component, there is no acoustic signal during x ray activation. Otherwise, the system is fully functional, and x ray is applied correctly. By means of the additional visual indicator (exposure LED light) the operator can monitor the x ray release. Also, after a successful x ray exposure, the clinical image is displayed on the monitor.
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?
Model Number 10273100 / UDI 04056869009117 Serial 1511 2168 2525 2633
- Product
- Mobilett Mira wireless (VA20) mobile x-ray system(s)
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 4 distributed in U.S.
- Distribution
- US Nationwide - Worldwide
- Recall date
- November 22, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)