{
  "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": "71735",
      "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": "Distributed in the states of CA. PA, VA, TX, MA, MD, WV, UT, FL, and TN.",
      "recall_number": "Z-2476-2015",
      "product_description": "0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only, Sterile Solution.",
      "product_quantity": "551 cases",
      "reason_for_recall": "Procedures for the acceptance and control of in-process product have not been adequately established.",
      "recall_initiation_date": "20150702",
      "center_classification_date": "20150827",
      "termination_date": "20170403",
      "report_date": "20150902",
      "code_info": "KH04143,exp. 07/2016;  KH04145, exp. 08/2016; KH04153, exp. 11/2016; KH04155, exp. 12/2016"
    }
  ]
}