{
  "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,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Austin",
      "address_1": "8700 Cameron Rd Ste 100",
      "reason_for_recall": "The product was packaged with the Instructions for Use for a different product (Ascension First Choice DRUJ System Partial Ulnar Head Implant).",
      "address_2": "",
      "product_quantity": "",
      "code_info": "170691",
      "center_classification_date": "20190201",
      "distribution_pattern": "Distributed to accounts in MO. Foreign distribution to Korea and Thailand.",
      "state": "TX",
      "product_description": "Ascension Modular Radial Head (MRH) Radial Head Implant, Catalog Number, MRH-350-04-WW",
      "report_date": "20190213",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Ascension Orthopedics, Inc",
      "recall_number": "Z-0794-2019",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "81782",
      "termination_date": "20191122",
      "more_code_info": "",
      "recall_initiation_date": "20181116",
      "postal_code": "78754-3947",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}