{
  "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-2542-2017",
      "product_description": "Sutures.  MAXON: MAXON 4/0 5X18\" GREEN CV-24 D-TACH; Item Number: 8886621933; MAXON 5/0 5X18 GR CV-23 D-TACH; Item Number: XX2109; MAXON* 4/0 5X30 GREEN V-20  D*TACH; Item Number: 8886603433",
      "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": "MAXON 4/0 5X18\" GREEN CV-24 D-TACH  D4K0396X  D4K2053X  D4L0541X  D4L1084X  D4L1272X  D4M0394X  MAXON 5/0 5X18 GR CV-23 D-TACH  D4K1485X  MAXON* 4/0 5X30 GREEN V-20  D*TACH  D4L1156GX"
    }
  ]
}