{
  "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": [
    {
      "status": "Terminated",
      "city": "Morrisville",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83070",
      "recalling_firm": "Suntech Medical, Inc.",
      "address_1": "507 Airport Blvd Ste 117",
      "address_2": "N/A",
      "postal_code": "27560-8200",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Pakistan",
      "recall_number": "Z-2277-2019",
      "product_description": "SunTech Medical Disposable, Neonate #4, 1-Tube, Male Bayonet, Blood Pressure Cuffs, Box of 20",
      "product_quantity": "80 total cuffs affected; 4 Boxes of 20 cuffs",
      "reason_for_recall": "Product is mislabeled. The label on the package is for a size #4 cuff, but the incorrect size #3 cuff was placed in the package.",
      "recall_initiation_date": "20190603",
      "center_classification_date": "20190814",
      "termination_date": "20201216",
      "report_date": "20190821",
      "code_info": "Catalog # 98-0400-98  Lot Number:   A4H201"
    }
  ]
}