FDAFDA · Food and drugs·Recall number Z-1061-2022
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
Published May 18, 2022 · Recall initiated: April 1, 2022
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failure to achieve the expected six-log reduction in microorganisms following the disinfection process.
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- Karl Storz Endoscopy
- Distributor
- 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
- Lot
- 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.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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