FDA Recalls KliniTray Model 2001155-F Surgical Device for Microbial Contamination Risk
The FDA has recalled KliniTray tissue examination boards (Model 2001155-F) due to potential microbial contamination. These surgical devices are used to position and examine tissue samples during procedures.
- Product
- KliniTray Platte Faxitron ,groB "R" sterile. Tissue resection margin examination board/large Model Number: 2001155-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact
- Category
- Medical Device
- Distribution
- Distributed nationwide