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Recall Observatory FDA recall evidence

Device product

CYSTO-URETHRO-FIBERSCOPE REF 11272C1 CYSTOSCOPE, 15FR X 370MM, ADULT REF 11272C2 and Kit Number 11272CK2 CYSTO-URETHRO-FIBERSCOPE REF 11272CU1 and Kit Number 11272CUK1

Z-1061-2022

April 01, 2022

Class II

Product summary

Firm
Karl Storz Endoscopy
Event
Event 89880
Status
Ongoing
Classification
Class II
Quantity
All Serial Numbers manufactured/distributed since January 2018
Official record key
device-enforcement:Z-1061-2022

Official wording

Reason: Failure to achieve the expected six-log reduction in microorganisms following the disinfection process.

Code information: 11272C1 n/a Flexible Cysto-Urethroscope Fiberscope Z18449US-BD (08-2018) UDI Code: 4048551226100; 11272C2 11272CK2 Flexible Cystoscope Z18449US-BD (08-2018) UDI Code: 4048551226100; 11272CU1 11272CUK1 Flexible Cystoscope Z18449US-BD (08-2018) UDI Code: 4048551226162; All Serial Numbers manufactured/distributed since January 2018.

Distribution pattern: U.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, Guam, 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, and WY. O.U.S.: Mexico, Lebanon, and South Korea

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Failure to achieve the expected six-log reduction in microorganisms following the disinfection process.