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Karl Storz Endoscopy recalls Karl Storz SE & CO. KG, REF 11003MB, Grasping Forceps, Flexible 1 mm, Rx Only
Recalled April 10, 2024 · FDA recall Z-1472-2024 · Karl Storz Endoscopy
Hazard
Inadequate reprocessing validation evidence · FDA Class II
Units
190 units
Sold at
US Nationwide distribution in the states of AR, CA, CO, CT, DC, FL, GA, IA, IL, LA, MA, MI, MN, MO , ND, NY, OH, OR, SD, TN, TX, UT, VA, WA, WV.
Description
Inadequate reprocessing validation evidence
Product
Karl Storz SE & CO. KG, REF 11003MB, Grasping Forceps, Flexible 1 mm, Rx Only
Manufacturer(s)
Karl Storz Endoscopy
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →