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Karl Storz Endoscopy recalls Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE
Recalled January 22, 2025 · FDA recall Z-0837-2025 · Karl Storz Endoscopy
Hazard
Due to failure of manual cleaning validation, biopsy and grasping forceps like sterility assurance. · FDA Class II
Units
285 units
Sold at
US: AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NY, OH, OR, PA, SC, TX, VA OUS: None
Description
Due to failure of manual cleaning validation, biopsy and grasping forceps like sterility assurance.
Product
Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE
Manufacturer(s)
Karl Storz Endoscopy
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →