{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Trumbull",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82663",
      "recalling_firm": "CooperSurgical, Inc.",
      "address_1": "95 Corporate Dr",
      "address_2": "N/A",
      "postal_code": "06611-1350",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Foreign: Denmark, Italy, Sweden",
      "recall_number": "Z-1367-2019",
      "product_description": "ICSI MICROPIPETTE  CooperSurgical part number: MICC001-30-B1.0",
      "product_quantity": "480 units",
      "reason_for_recall": "ICSI CUSTOM MICROPIPETTES the thirty-degree bend is absent",
      "recall_initiation_date": "20190327",
      "center_classification_date": "20190517",
      "termination_date": "20200501",
      "report_date": "20190529",
      "code_info": "Lot 1557"
    }
  ]
}