{
  "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": [
    {
      "country": "United States",
      "city": "Portage",
      "address_1": "4100 E Milham Ave",
      "reason_for_recall": "Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable rates.",
      "address_2": "",
      "product_quantity": "1244",
      "code_info": "1. Lot Number: 17278012; 2. Lot Numbers: 17278012, 17278022, 17279022, 17282012, 17282022, 17291012, 17291022      UDI: (01)4546540593108;  (01)7613252039259",
      "center_classification_date": "20180328",
      "distribution_pattern": "Distributed in all 50 U.S. States and the District of Columbia. Distributed in Australia, Argentina, Japan, Canada, Chile, Korea, Spain, France, Italy, Netherlands, and United Kingdom.",
      "state": "MI",
      "product_description": "1. AutoPlex System, Product Number: 0605-887-000, UDI: (01)4546540593108; 2. AutoPlex System: w/ VertaPlex HV, Product Number: 0607-687-000, UDI: (01)7613252039259   Bone cement.",
      "report_date": "20180404",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Instruments Div. of Stryker Corporation",
      "recall_number": "Z-1250-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "79418",
      "termination_date": "20190416",
      "more_code_info": "",
      "recall_initiation_date": "20171109",
      "postal_code": "49002-9704",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}