{
  "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": "Center Valley",
      "address_1": "3773 Corporate Pkwy",
      "reason_for_recall": "There is a potential for the needle to detach from the suture thread during surgery.  If the needle becomes detached the defective suture will need to be replaced causing the wound to be sutured a second time.",
      "address_2": "",
      "product_quantity": "180 units",
      "code_info": "Lot # 115441  Product Code C1046619",
      "center_classification_date": "20161026",
      "distribution_pattern": "Distributed in Arizona",
      "state": "PA",
      "product_description": "Safil QUI + UNDY 5/0 (1) 45CM DSMP13 Suture",
      "report_date": "20161102",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Aesculap Implant Systems LLC",
      "recall_number": "Z-0316-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75142",
      "termination_date": "20180216",
      "more_code_info": "",
      "recall_initiation_date": "20160801",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}