{
  "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": "Nashville",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71175",
      "recalling_firm": "MRP, LLC dba AMUSA",
      "address_1": "5209 Linbar Dr Ste 640",
      "address_2": "N/A",
      "postal_code": "37211-1026",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution in states of:OH, PA, AL, IL, TN, and CT.",
      "recall_number": "Z-1709-2015",
      "product_description": "0.9% Sodium Chloride Injection, USP, Flush Syringe, 10 mL in 12 mL, Sterile, Rx only, Code No. 2T0806    Usage: Flush syringe.",
      "product_quantity": "200,000 units",
      "reason_for_recall": "Incorrect expiration date on label",
      "recall_initiation_date": "20150427",
      "center_classification_date": "20150604",
      "termination_date": "20160502",
      "report_date": "20150610",
      "code_info": "CODES:  KH04103, KH04104, KH04105"
    }
  ]
}