{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Dublin",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89524",
      "recalling_firm": "Carl Zeiss Meditec, Inc.",
      "address_1": "5300 Central Parkway",
      "address_2": "N/A",
      "postal_code": "94568",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "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",
      "recall_number": "Z-0723-2022",
      "product_description": "CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex",
      "product_quantity": "1,272 devices",
      "reason_for_recall": "Optic nerve head angiography scan to be turned off due to its distribution without pre-market clearance.",
      "recall_initiation_date": "20220114",
      "center_classification_date": "20220304",
      "report_date": "20220316",
      "code_info": "All instrument serial numbers running running software versions 11.5, 11.5.1 and 11.5.2. with ONH Angiography 4.5x4.5mm Scan"
    }
  ]
}