Z-0723-2022 Class II Ongoing

Recalled by Carl Zeiss Meditec, Inc. — Dublin, CA

Recall Details

Product Type
Devices
Report Date
March 16, 2022
Initiation Date
January 14, 2022
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1,272 devices

Product Description

CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex

Reason for Recall

Optic nerve head angiography scan to be turned off due to its distribution without pre-market clearance.

Distribution Pattern

U.S Nationwide Distribution.: OH, CA, IN, AR, IA, LA, WI, OK, IL, OR, AL, KY, WY, WA, MN, NE, PA, SD, AZ, PR, TN, GA, FL, DE, NY, NH, TX, MS, MA, NV, UT, WV, ME, CO, AK, NM, KS, MO, MI, MD, ID, CT, NJ, MT, NC, VA, HI, VT, ND, SC, DC, RI

Code Information

All instrument serial numbers running running software versions 11.5, 11.5.1 and 11.5.2. with ONH Angiography 4.5x4.5mm Scan