Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps Recalled by Karl Storz Endoscopy Due to Due to failure of manual cleaning validation, biopsy...
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 Karl Storz Endoscopy directly.
Affected Products
Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE
Quantity: 285 units
Why Was This Recalled?
Due to failure of manual cleaning validation, biopsy and grasping forceps like sterility assurance.
Where Was This Sold?
This product was distributed to 32 states: AZ, AR, CA, CO, CT, FL, GA, HI, ID, IL, IN, IA, KY, LA, MD, MA, MI, MN, MS, MO, MT, NE, NJ, NM, NY, NC, OH, OR, PA, SC, TX, VA
About Karl Storz Endoscopy
Karl Storz Endoscopy has 70 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report