Cios Spin Image-Intensified Fluoroscopic X-Ray System, Model Numbers VA30-10308194
Reported: June 3, 2020 Initiated: April 17, 2020 #Z-2128-2020
Product Description
Cios Spin Image-Intensified Fluoroscopic X-Ray System, Model Numbers VA30-10308194
Reason for Recall
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.
Details
- Recalling Firm
- Siemens Medical Solutions USA, Inc
- Units Affected
- 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.
- Location
- Malvern, PA
Frequently Asked Questions
What product was recalled? ▼
Cios Spin Image-Intensified Fluoroscopic X-Ray System, Model Numbers VA30-10308194. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 20.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 3, 2020. Severity: Moderate. Recall number: Z-2128-2020.
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