{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Co. Longford",
      "state": "",
      "country": "Ireland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81632",
      "recalling_firm": "Abbott Ireland Diagnostics Division",
      "address_1": "Lisnamuck",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "AR, FL, GA, MD, OK, VA",
      "recall_number": "Z-0668-2019",
      "product_description": "Alinity i Progesterone Reagent Kit, List Number 08P3620",
      "product_quantity": "157 units",
      "reason_for_recall": "Abbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A.  If a bottle neck is damaged, it may cause a failure during the reagent loading process on the Alinity i instrument.",
      "recall_initiation_date": "20181121",
      "center_classification_date": "20181222",
      "termination_date": "20210401",
      "report_date": "20190102",
      "code_info": "UDI/Lot Numbers  (01)00380740121877 (17)190503(10) 91254UI00 / 91254UI00  (01)00380740121877 (17)190618(10)92360UI00 / 92360UI00",
      "more_code_info": ""
    }
  ]
}