{
  "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": "Austin",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77930",
      "recalling_firm": "Encore Medical, Lp",
      "address_1": "9800 Metric Blvd",
      "address_2": "N/A",
      "postal_code": "78758-5445",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "OH, VA",
      "recall_number": "Z-3102-2017",
      "product_description": "MODIFIED/SPECIAL INSTRUMENT, TURON GLENOID REAMER, REAM AND RUN, Catalog Numbers:    REF S-200956 - 5mm PIN, SIZE 46   REF S-200957 - 5mm PIN, SIZE 50  REF S-200958 - 5mm PIN, SIZE 58",
      "product_quantity": "5 units",
      "reason_for_recall": "It was reported that the models used to manufacture S-200956/958 had the wrong dimension used to create the spherical radius cutting surface. Device design allows a larger spherical radius cutting surface than intended.",
      "recall_initiation_date": "20170804",
      "center_classification_date": "20170830",
      "termination_date": "20230628",
      "report_date": "20170906",
      "code_info": "Catalog number, Lot Number  S-200956, 535U1000  S-200957, 536U1000  S-200958, 537U1000"
    }
  ]
}