Karl Storz Endoscopy: Medical Device Recall in 2024 - (Recall #: Z-3224-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Karl Storz - Endoskope , REF: 27830KA, Nephroscope for MIP M, Rx only, CE 0123

Product Classification:

Class II

Date Initiated: July 23, 2024

Date Posted: October 2, 2024

Recall Number: Z-3224-2024

Event ID: 95220

Reason for Recall:

Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

Status: Ongoing

Product Quantity: 5 units

Code Information:

All Lots/UDI: (01)04048551234099

Distribution Pattern:

US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY, Puerto Rico, Guam.

Voluntary or Mandated:

Voluntary: Firm initiated