{
  "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": "Oberkochen",
      "state": "",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89928",
      "recalling_firm": "Carl Zeiss Meditec AG",
      "address_1": "Rudolf-Eber-Str. 11",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "U.S.: AL, AR, AZ, CA, CT, FL, GA, IA, IL, KS, LA, MA, MD, MI, MN, MO, MS, MT, NC, NJ, NY, OH, OR, PA, Puerto Rico, SC, TN, TX. UT, VA, WA, and WV  O.U.S.: Not provided",
      "recall_number": "Z-1007-2022",
      "product_description": "ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.",
      "product_quantity": "1225 devices",
      "reason_for_recall": "High friction of the slider can cause the device to stick, or not move as intended.",
      "recall_initiation_date": "20220316",
      "center_classification_date": "20220426",
      "report_date": "20220504",
      "code_info": "Model: 303071-9090-000 Catalog Number: FG-50608 UDI: (01)04049539104496(11)201102(17)231031(10)FG21082410 Lot Number: FG21082410",
      "more_code_info": ""
    }
  ]
}