{
  "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": "90789",
      "recalling_firm": "Abbott Molecular, Inc.",
      "address_1": "1300 E Touhy Ave",
      "address_2": "N/A",
      "postal_code": "60018-3315",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was made to AZ, CA, CT, FL, GA, IL, KS, KY, LA, MA, MI, MN, MO, NC, NJ, NV, NY, OK, PA, RI, TN, TX, WA, and WI.  There was government distribution but no military distribution.  Foreign distribution was made to Chile and Taiwan.",
      "recall_number": "Z-1679-2022",
      "product_description": "Abbott Alinity m SARS-CoV-2 CTRL Kit, REF 09N78-085, each kit contains 12 x 1.3mL CTRL - and 12 x 1.3 mL CTRL +, For In Vitro Diagnostic Use.",
      "product_quantity": "579 kits",
      "reason_for_recall": "Reports received of an increase of message code 9186 (internal control failed) when using the kit.",
      "recall_initiation_date": "20220819",
      "center_classification_date": "20220906",
      "report_date": "20220914",
      "code_info": "Lot #530738, UDI (01)00884999049208(10)530738(17)230527(240)09N78-085."
    }
  ]
}