{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "North Haven",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71893",
      "recalling_firm": "Covidien LLC",
      "address_1": "60 Middletown Ave",
      "address_2": "N/A",
      "postal_code": "06473-3908",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-2525-2015",
      "product_description": "Monoject 0.9% Saline Flush Prefill Double Pouch  Item Code: 8881570129  Product Usage:  Sterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling intravascular access devices.",
      "product_quantity": "207,876",
      "reason_for_recall": "Sterility may be compromised",
      "recall_initiation_date": "20150806",
      "center_classification_date": "20150901",
      "termination_date": "20170629",
      "report_date": "20150909",
      "code_info": "Lot Numbers:  P15035  P15036  P15037  P15041  P15042  P15046  P15047  P15048  P15049  P15056  P15057  P15058  P15059  P15063  P15064  P15069  P15070  P15071  P15078  P15079  P15080  P15081  P15091"
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}