{
  "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": [
    {
      "country": "United States",
      "city": "Minneapolis",
      "address_1": "614 McKinley Pl NE",
      "reason_for_recall": "The kit was provided without a copy of the lot-specific kit booklet and the Calibrator 0 vial 18D1/4 label incorrectly specified reconstitution volume of 2mL.",
      "address_2": "",
      "product_quantity": "8 kits",
      "code_info": "Manufacturing Lot # 182801",
      "center_classification_date": "20181108",
      "distribution_pattern": "IA and CO",
      "state": "MN",
      "product_description": "R&D systems, a bio-techne brand Human Total 25-OH Vitamin D IVD ELISA Kit, REF RDKAP1971",
      "report_date": "20181114",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "R & D Systems, Inc.",
      "recall_number": "Z-0410-2019",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "81121",
      "termination_date": "20200901",
      "more_code_info": "",
      "recall_initiation_date": "20180911",
      "postal_code": "55413-2610",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}