{
  "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": "2026-04-15",
    "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": "71238",
      "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": "Nationwide and Canada, Australia, Germany, New Zealand, Japan, India, Great Britain",
      "recall_number": "Z-1752-2015",
      "product_description": "Gyrus ACMI Diego Elite Tubeset; intended for cutting, coagulation, drilling, debriding, and removal of bone, and soft and hard tissue in general ENT, Sinus/Rhinology, Nasopharyngeal/Laryngology, and Head & Neck procedures. Catalog No. TS100S, Lot numbers JC929332 and below, Rx Only, STERILE EO",
      "product_quantity": "12,020 boxes",
      "reason_for_recall": "Potential lack of sterility assurance.",
      "recall_initiation_date": "20150508",
      "center_classification_date": "20150611",
      "termination_date": "20160517",
      "report_date": "20150617",
      "code_info": "Lot number:  JC929332"
    }
  ]
}