{
  "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": "Danvers",
      "address_1": "35-37A Cherry Hill Drive",
      "reason_for_recall": "Two reports have been received on the 6F launcher Guide Catheter lot (Model Number LA6JR40K; lot No 0007244836} for incorrect usable length of the Guide Catheter. It was reported that the catheters had a usable length of 90 cm instead of 55 cm, which was specified on the packaging label. Usable length is defined as the total length of catheter shaft from the distal end of the strain relief to the",
      "address_2": "",
      "product_quantity": "11 devices",
      "code_info": "Lot Number:  0007244836  MODEL: LA6JR40K",
      "center_classification_date": "20141113",
      "distribution_pattern": "US Distribution including the states of NC, IA, IL and KS.",
      "state": "MA",
      "product_description": "Medtronic Launcher Coronary Guide Catheter; MODEL: LA6JR40K",
      "report_date": "20141119",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Vascular",
      "recall_number": "Z-0205-2015",
      "initial_firm_notification": "Visit",
      "product_type": "Devices",
      "event_id": "69488",
      "termination_date": "20150218",
      "more_code_info": "",
      "recall_initiation_date": "20141013",
      "postal_code": "01923-2565",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}