{
  "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": [
    {
      "status": "Terminated",
      "city": "Mansfield",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65978",
      "recalling_firm": "Covidien LLC",
      "address_1": "15 Hampshire Street",
      "address_2": "N/A",
      "postal_code": "02048-1113",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA Nationwide and the country of  Bermuda",
      "recall_number": "Z-2178-2013",
      "product_description": "Monoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 10 mL Fill  Product ID: 8881570121    Product Usage:  Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous administration sets and indwelling intravenous access devices",
      "product_quantity": "3,235,860 units",
      "reason_for_recall": "Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin",
      "recall_initiation_date": "20130816",
      "center_classification_date": "20130910",
      "termination_date": "20151021",
      "report_date": "20130918",
      "code_info": "Lot Numbers:   13A0084N  13A0094  13B0364  13C0514",
      "more_code_info": ""
    }
  ]
}