Stingray Surgical Recalls Bipolar Forceps Due to Uncleared Instructions
Stingray Surgical Products is recalling bipolar forceps because the Instructions For Use were altered without FDA clearance.
- Product
- Bipolar Forceps model number: S02-XXX, S03-XXX, P02-XXX, and P03-XXX. "Instructions For Use" (QF7.5.1A.R01 thru QF7.5.1A.R06 Care and Handling of Bipolar Forceps. Bipolar Forceps designed to grasp, manipulate and coagulate selected tissue for use in general surgical procedure
- Category
- Medical Device
- Distribution
- Distributed nationwide