AXIOM Vertix MD Trauma systems radiographic X-ray recall
AXIOM Vertix MD Trauma systems radiographic X-ray
Why was AXIOM Vertix MD Trauma systems radiographic X-ray recalled?
There is a potential issue and possible hazard to patients when using the AXIOM Vertix MD Trauma systems. In rare cases, steel ropes inside the lift column of the system can be defective without triggering the safety lock, which can result in the U-arm dropping down unexpectedly during movement in vertical direction, potentially causing serious injury.
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?
AXIOM Vertix MD Trauma systems (material no. 08908290) with serial numbers 1022 through 1058.
- Product
- AXIOM Vertix MD Trauma systems radiographic X-ray
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 2
- Distribution
- US Distribution including MO and OH.
- Recall date
- April 23, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)