{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Nashville",
      "address_1": "5209 Linbar Dr Ste 640",
      "reason_for_recall": "Incorrect labeling of the expiration date",
      "address_2": "",
      "product_quantity": "1,080 units (3 cases)",
      "code_info": "KH04090",
      "center_classification_date": "20150615",
      "distribution_pattern": "US distribution to CA only.",
      "state": "TN",
      "product_description": "T/S2 0.9% Sodium Chloride Injection, USP, AMUSA Sterile Field Flush Syringe, 10 mL in 12 mL Single Use Syringe, Rx only, Part no. 2S0706    Usage: Flush syringe.",
      "report_date": "20150624",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "MRP, LLC dba AMUSA",
      "recall_number": "Z-1808-2015",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "70974",
      "termination_date": "20150622",
      "more_code_info": "",
      "recall_initiation_date": "20150209",
      "postal_code": "37211-1026",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}