{
  "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": "Southborough",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65255",
      "recalling_firm": "Gyrus Acmi, Incorporated",
      "address_1": "136 Turnpike Road",
      "address_2": "N/A",
      "postal_code": "01772-2118",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and countries of: Canada and United Kingdom.",
      "recall_number": "Z-1439-2013",
      "product_description": "GYRUS ACMI, MYRINGOTOMY KNIFE DISPOSABLE, SICKLE BLADE FLAT HANDLE, REF 130715, Rx only, STERILE EO, GYRUS ACMI, INC., 136 TURNPIKE ROAD, SOUTHBOROUGH, MA  01722-2104    Disposable myringotomy knife intended to perforate the tympanic membrane to allow the placement of a bent tube or to directly provide ventilation or drainage of the middle ear.",
      "product_quantity": "100 boxes of 6 units",
      "reason_for_recall": "lack of sterility assurance",
      "recall_initiation_date": "20130524",
      "center_classification_date": "20130531",
      "termination_date": "20140530",
      "report_date": "20130612",
      "code_info": "JC477666"
    }
  ]
}