{
  "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": "2026-04-29",
    "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": "63629",
      "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 state of Kansas and country of Korea.",
      "recall_number": "Z-0411-2013",
      "product_description": "PARPARELLA-TYPE VENT TUBE, 1.02 MM,  SILICONE, REF 240044, QTY 6, Rx Only, STERILE EO, GYRUS ACMI INC.,    Tympanostomy tube",
      "product_quantity": "10 boxes/60 units",
      "reason_for_recall": "One lot of tympanostomy tubes were manufactured with silicon that was found to be contaminated with ethylene vinyl acetate copolymer.",
      "recall_initiation_date": "20121017",
      "center_classification_date": "20121120",
      "termination_date": "20130409",
      "report_date": "20121128",
      "code_info": "JC470075"
    }
  ]
}