{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Elkton",
      "address_1": "950 Elkton Blvd",
      "reason_for_recall": "According to the Terumo (TMC) this device is used to access the human peripheral vascular system for short term use (less than 30 days) for the purpose of infusing fluids into patients.  A small percentage of the catheters in the affected lots may have damage to the ETFE catheter which may allow the catheter to break during withdrawal.",
      "address_2": "",
      "product_quantity": "2,478,200",
      "code_info": "PRODUCT CODE    3SR-OX2225CA  3SR-OX2419CA  3SR-OX2225CA  3SR-OX2419CA  SR-TL2419M  3SR-OX2419CA  3SR-OX2225CA  SR-TL2225M  3SR-OX2225CA  3SR-OX2419CA  3SR-OX2225CA  3SR-OX2419CA  SR-TL2419M  3SR-OX2225CA  3SR-OX2225CA  3SR-OX2225CA  3SR-OX2225CA  SR-TL2225M  3SR-OX2225CA  3SR-OX2225CA  3SR-OX2225CA  3SR-OX2419CA  SR-TL2419M  3SR-OX2419CA  3SR-OX2419CA  3SR-OX2419CA    LOT NUMBER    RF2727  RF2727  RG0227  RG0927  RG0927  RG1627  RG2027  RG2027  RG2327  RH0727  RH1427  RH1427  RH1427  RH2127  RH2827  RH3127  RK0427  RK0427  RK1127  RK1827  RK2527  RL0227  RL0227  RL0827  RL1527  RL2227",
      "center_classification_date": "20170501",
      "distribution_pattern": "US Distribution.    This product has been sold to both distribution companies with multiple locations and directly to end users/hospitals in US.",
      "state": "MD",
      "product_description": "SurFlo IV Catheter",
      "report_date": "20170510",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Terumo Medical Corporation",
      "recall_number": "Z-1896-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76948",
      "termination_date": "20170501",
      "more_code_info": "",
      "recall_initiation_date": "20150805",
      "postal_code": "21921-5322",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}