{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Des Plaines",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91777",
      "recalling_firm": "Abbott Molecular, Inc.",
      "address_1": "1300 E Touhy Ave",
      "address_2": "",
      "postal_code": "60018-3315",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "US Distribution to state of:  PA, a government account.",
      "recall_number": "Z-1349-2023",
      "product_description": "Abbott Alinity m System, REF 08N53-002, containing Amplification Detetction Unit (ADU) #4.",
      "product_quantity": "1",
      "reason_for_recall": "The instrument was found to be installed without plunger assemblies in the clamp bar for an Amplification Detection Unit.  After correction of the issue, the instrument was returned for use without calibration.  This would result in a potential for delay of results and incorrect results.",
      "recall_initiation_date": "20221111",
      "center_classification_date": "20230406",
      "report_date": "20230412",
      "code_info": "Alinity m System Serial #01015, UDI: (01)00884999048034(11)220505(21)01015(240)08N53-002; ADU Serial #AMP05139.",
      "more_code_info": ""
    }
  ]
}