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Smith & Nephew, Inc., Endoscopy Div.

Smith & Nephew, Inc., Endoscopy Div. Recalls

All product recalls associated with Smith & Nephew, Inc., Endoscopy Div..

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Recall Summary

Total Recalls

232

Past Year

Class I (Serious)

Most Recent

Nov 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 221–232 of 232 recalls

Smith & Nephew, Inc., Endoscopy Div.: Smith & Nephew Grasper, Cupped 3.4mm REF: 011014

Cupped Grasper Handle marked incorrectly as Duckbill Upbiter

FDAApr 6, 2005CA, MA, OH +1 more• Smith & Nephew, Inc., Endoscopy Div.

Smith & Nephew, Inc Endoscopy Division: Smith & Nephew TRIVEX System Pneumatic Footswitch, Part #...

Build-up of static charge in Pneumatic Footswitch tubing may cause control unit to reset to default settings in the operating room during surgery.

FDAOct 12, 2004Nationwide• Smith & Nephew, Inc Endoscopy Division

Smith & Nephew Inc: Tibial Base Plates

The firm received confirmed reports of Genesis Uni Articular Inserts not locking into tibial base plates intraoperatively.

FDAJun 21, 2004Nationwide

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• Smith & Nephew Inc

Smith & Nephew Inc: Genesis Uni Articular Inserts

The firm received confirmed reports of Genesis Uni Articular Inserts not locking into tibial base plates intraoperatively.

FDAJun 21, 2004Nationwide• Smith & Nephew Inc