Ziehm Vision RFD 3D Mobile C-arm for Mobile recall
Ziehm Vision RFD 3D Mobile C-arm for Mobile Fluoroscopic Imaging
Why was Ziehm Vision RFD 3D Mobile C-arm for Mobile recalled?
Malfunction of the radiation-warning timer and the 3D-specific interval warning. No 5-minute timer dialogs or beeper will occur until the unit is rebooted.
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?
Serial #'s 20628, 20657, 20658, 20659, 20660, 20671, 20672, 20678, 20679, 20680, 20681, 20682, 20683, 20684, 20685, 20686, 20687, 20712, 10713, 20714, 20715, 20717, 20718, 20722, 20723, 20724, 20725, 20726, 20772, 20793, and 20794.
- Product
- Ziehm Vision RFD 3D Mobile C-arm for Mobile Fluoroscopic Imaging
- Recalling firm
- Ziehm Imaging Inc
- Quantity
- 31 devices
- Distribution
- US Distribution including Puerto Rico and to the states of :FL, GA, VA,MA. ME, MI, NY, NJ, PA, RI, IL, TX, AZ, CA, NV, UT, and WA.
- Recall date
- August 31, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)