Karl Storz Endoscopy recalls Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE
- Recall date
- December 19, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0837-2025
- FDA classification
- Class II
- Brand / firm
- Karl Storz Endoscopy
- Sold / distributed
- 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
Why it was recalled
Due to failure of manual cleaning validation, biopsy and grasping forceps like sterility assurance.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE
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