Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bipolar Forceps model number: S02-XXX Recalled by Stingray Surgical Products, LLC Due to On 05/23/2012, Stingray Surgical Products, LLC., Boca Raton,...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stingray Surgical Products, LLC directly.
Affected Products
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 procedures powered by a high frequency generator.
Quantity: 6326
Why Was This Recalled?
On 05/23/2012, Stingray Surgical Products, LLC., Boca Raton, FL initiated a recall initiated due to "Instructions For Use" of Bipolar Forceps not being cleared by FDA and incorrect "Instructions For Use" . The sterilization instructions have been altered without the clearance of the FDA.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stingray Surgical Products, LLC
Stingray Surgical Products, LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report