Cios Spin Image-Intensified Fluoroscopic X-Ray System recall
Cios Spin Image-Intensified Fluoroscopic X-Ray System, Model Numbers VA30-10308194
Why was Cios Spin Image-Intensified Fluoroscopic X-Ray System recalled?
The unplugging of the main cable on the monitor trolley from the X10 connector can cause an unsafe electrical voltage (up to 67,6 V DC) at the X10 connector. This can result in an electrical shock if the user or other persons touch the contact pins of the X10 connector.
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 Numbers: 50135 50131 50171 50129 50048 50184 50180 50136 50185 50153 50155 50130 50127 50134 50166 50192 50161 50128 50132 50160
- Product
- Cios Spin Image-Intensified Fluoroscopic X-Ray System, Model Numbers VA30-10308194
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 20
- Distribution
- US Nationwide Distribution to states of: AR, AZ, CA, FL, IL, IN, MA, MD, MI, MN, NC, NE, NH, NJ, NY, OH, OK, SC, TN, TX, UT, VA, WA, and Puerto Rico.
- Recall date
- June 3, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)