{
  "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": [
    {
      "status": "Terminated",
      "city": "Franklin",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72695",
      "recalling_firm": "Arthrosurface, Inc.",
      "address_1": "28 Forge Pkwy",
      "address_2": "N/A",
      "postal_code": "02038",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of : PA, WV and CA.",
      "recall_number": "Z-0475-2016",
      "product_description": "Total Toe Instrument Kit, Labeled in part: \"Instrument Set, 15mm Toe, Dorsal Flange Combi\" Part Number: 9000-3002     The component in question is the hex driver (part number 2009-4001).",
      "product_quantity": "3 units",
      "reason_for_recall": "An oversight in the implementation of the design change record resulted in outdated components being shipped to customers. The component did not pass a half-cycle sterilization.",
      "recall_initiation_date": "20140609",
      "center_classification_date": "20151223",
      "termination_date": "20160205",
      "report_date": "20151230",
      "code_info": "SN 000242  SN 000244  SN 000246  SN 000247"
    }
  ]
}