Luminos dRF with software VD10- A diagnostic imaging recall
Luminos dRF with software VD10- A diagnostic imaging system for radiographic and fluoroscopic studies Model Number: 10094200
Why was Luminos dRF with software VD10- A diagnostic imaging recalled?
Potential risk of collision with the ceiling, wall, or objects which may result in serious injury to staff or patients due to room configuration parameters of the system being set to default values
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?
UDI: N/A S/N: 4650 Expanded Recall 2/24/23: 4043 4051 4143 4156 4199 4201 4238 4252 4291 4323 4332 4342 4354 4372 4401 4430 4508 4600 4606 4637 4641 4683 4722 4724 4734
- Product
- Luminos dRF with software VD10- A diagnostic imaging system for radiographic and fluoroscopic studies Model Number: 10094200
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 1 unit; Expanded Recall: 25 units
- Distribution
- US Nationwide distribution.
- Recall date
- March 1, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)