{
  "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": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84698",
      "recalling_firm": "QUIDEL CARDIOVASCULAR INC",
      "address_1": "9975 Summers Ridge Rd",
      "address_2": "N/A",
      "postal_code": "92121-2997",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US:  ID, FL, GA, IL, TX, KY, MO, AL, UT, IA, WA, OH, AZ, NY, OK, OR, IN, KS    Non-US:  CA, NL",
      "recall_number": "Z-1552-2020",
      "product_description": "Quidel Triage TOX Drug Screen Control 1   Kit Box containing 5 Control 1 vials with 5 x 0.25 mL vials per box.    Quidel Cardiovascular Inc.  9975 Summers Ridge Road  San Diego, CA 92121 USA  Quidel.com",
      "product_quantity": "123 kits",
      "reason_for_recall": "Due to an error in the programming of the Control CODE CHIP module for this lot, a failing result is inappropriately displayed for AMP and mAMP. This issue results in the Triage Meter displaying a failing control result for the AMP and mAMP tests when the control did  not fail.",
      "recall_initiation_date": "20190409",
      "center_classification_date": "20200320",
      "termination_date": "20210114",
      "report_date": "20200401",
      "code_info": "Lot Number: C3470AN  Part Number 94413",
      "more_code_info": ""
    }
  ]
}