{
  "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
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  },
  "results": [
    {
      "country": "United States",
      "city": "Mahwah",
      "address_1": "325 Corporate Dr",
      "reason_for_recall": "Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.",
      "address_2": "",
      "product_quantity": "241 units",
      "code_info": "Catalog No. 0930-9-003",
      "center_classification_date": "20160811",
      "distribution_pattern": "Worldwide Distribution - US Nationwide",
      "state": "NJ",
      "product_description": "Orthopedic manual surgical instrument    Usage:  Exeter Rasp Handle is a reusable instrument which is part of the Exeter femoral hip system. Exeter femoral rasps are assembled with the rasp handle and locked in place by closing down the lever on the rasp handle. The rasp handle is then used to guide the rasp into the patient\u0019s femur and is impacted using a mallet in order to remove bone and further prepare the femur.",
      "report_date": "20160817",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Howmedica Osteonics Corp.",
      "recall_number": "Z-2396-2016",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "74743",
      "termination_date": "20170608",
      "more_code_info": "",
      "recall_initiation_date": "20160701",
      "postal_code": "07430-2006",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}