{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Gainesville",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86630",
      "recalling_firm": "Exactech, Inc.",
      "address_1": "2320 NW 66th Ct",
      "address_2": "N/A",
      "postal_code": "32653-1630",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US consignees - AZ, CA, CO, FL, IL, IN, KY, LA, OH, OK, MD, ME, MN, NV, NY, SC, TN, TX, VA, WA, WI    International consignees - Australia, Japan, and United Kingdom",
      "recall_number": "Z-0460-2021",
      "product_description": "Catalog 314-13-33, Equinoxe Cage Glenoid, Posterior Augment, Right, Medium",
      "product_quantity": "40 devices",
      "reason_for_recall": "The product may be mislabeled.",
      "recall_initiation_date": "20201006",
      "center_classification_date": "20201117",
      "termination_date": "20231113",
      "report_date": "20201125",
      "code_info": "Catalog 314-13-33, Serial Numbers:  6259572  6259573  6259575  6259577  6259578  6259579  6259583  6259584  6259587  6259588  6259590  6259591  6259592  6259594  6259595  6132993  6132994  6132995  6132996  6132997  6132998  6132999  6133000  6133002  6133003  6133005  6133008  6133009  6133010  6133011  6133013  6133014  6133017  6133020  6133021  6133023  6133029  6133030  6133031  6133032"
    }
  ]
}