{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Canton",
      "address_1": "5449 Research Dr",
      "reason_for_recall": "Vials of the autoHDL/LDL Calibrator were shipped without a vial label.",
      "address_2": "",
      "product_quantity": "22",
      "code_info": "Lot Number 808801-180;  UDI: 00811727011411",
      "center_classification_date": "20181105",
      "distribution_pattern": "US Nationwide in the states of CA, FL, GA, MI, and OH.",
      "state": "MI",
      "product_description": "Pointe Scientific AutoHDL/LDL Cholesterol Calibrator, Catalog Number H7545-CAL - Product Usage: For the calibration of Pointe Scientific s autoHDL and autoLDL Cholesterol Reagent Set in serum or plasma. For in vitro diagnostic use only.",
      "report_date": "20181114",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Medtest Holdings, Inc.",
      "recall_number": "Z-0389-2019",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "81160",
      "termination_date": "20191204",
      "more_code_info": "",
      "recall_initiation_date": "20180810",
      "postal_code": "48188-2261",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}