{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "North Haven",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77144",
      "recalling_firm": "Medtronic",
      "address_1": "60 Middletown Ave",
      "address_2": "N/A",
      "postal_code": "06473-3908",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution.  US Nationwide including PR, and countries of AU, BE, CA, CL, CN, IL, IT, JP, KR, MX, PA, SA, SG, and TR.",
      "recall_number": "Z-2546-2017",
      "product_description": "USPACK-SUTURE KIT; Item Number: US1672",
      "product_quantity": "478,465 (total for all products)",
      "reason_for_recall": "Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.",
      "recall_initiation_date": "20170503",
      "center_classification_date": "20170614",
      "termination_date": "20190718",
      "report_date": "20170621",
      "code_info": "A5D0789X"
    }
  ]
}