Class II

Medical Device Recall: Karl Storz SE & CO. KG, REF 11003MB, Grasping Forceps, Flexible 1 mm, Rx Only

Karl Storz Endoscopy · February 27, 2024

Reason for Recall

Inadequate reprocessing validation evidence

Distribution

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.

States Affected

NATIONWIDE

Quantity Affected

190 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1472-2024

Status: ongoing

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Karl Storz Endoscopy Medical Device Recall: Karl Storz SE & CO. KG, REF 11003MB, Grasping Forceps, Flexible 1 mm, Rx Only | SafeCheck