{
  "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": "West Chester",
      "address_1": "1302 Wrights Ln E",
      "reason_for_recall": "Synthes is initiating a voluntary recall of the Flexible Grip (Part number 355.28) which is part of the Universal Nail System, due to the potential lack of the ability to thoroughly clean the instrument.",
      "address_2": "",
      "product_quantity": "328",
      "code_info": "Part number 355.28, all lot numbers",
      "center_classification_date": "20130405",
      "distribution_pattern": "Nationwide Distribution including the states of AZ, CA, CO, FL, IA, ID, GA, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, NC, NH, NJ, NV, NY, OH, PA, RI, TN, TX, UT, VT, WA, WI, and WV.",
      "state": "PA",
      "product_description": "Flexible Grip which is part of the Synthes Universal Nail System.    Indicated for the conventional (non-locking) technique of treating stable diaphyseal fractures.",
      "report_date": "20130417",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Synthes USA HQ, Inc.",
      "recall_number": "Z-1062-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64200",
      "termination_date": "20150831",
      "more_code_info": "",
      "recall_initiation_date": "20130111",
      "postal_code": "19380-3417",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}