{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.",
      "address_2": "",
      "product_quantity": "638 units",
      "code_info": "Item No. 814511420; Lot No. (Exp. Date) UDI: 535130 (06/02/2027) UDI (01)00887868039195 (17)270602 (10)535130; 858960 (06/15/2027) UDI (01)00887868039195 (17)270615 (10)858960",
      "center_classification_date": "20180129",
      "distribution_pattern": "US nationwide distribution. Also Portugal and the Netherlands.",
      "state": "IN",
      "product_description": "Affixus Hip Fracture Nail, RH 130 DEG 11MM X 420MM",
      "report_date": "20180207",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-0470-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "78763",
      "termination_date": "20190329",
      "more_code_info": "",
      "recall_initiation_date": "20170807",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}