FDA Enforcement Class II Ongoing

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

Recall: Z-1061-2022 · Reported May 18, 2022

Enforcement

Recall Number
Z-1061-2022
Event ID
89880
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Karl Storz Endoscopy
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Report Date
May 18, 2022
Initiation Date
April 1, 2022
Classification Date
May 12, 2022
Address
2151 E Grand Ave, N/A, El Segundo, CA, 90245-5017, United States

Description

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

Reason

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

Code Info

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

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

Quantity

All Serial Numbers manufactured/distributed since January 2018