{
  "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
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Malvern",
      "address_1": "45 Great Valley Pkwy",
      "reason_for_recall": "Two isolated instances of holes in the outer header bag component of the double barrier sterile packaging configuration",
      "address_2": "",
      "product_quantity": "9805",
      "code_info": "All lots, Model Number of device: 2090-0501, 2090-0502, 2090-0504,  2090-0505",
      "center_classification_date": "20150916",
      "distribution_pattern": "Worldwide Distribution - Nationwide Distribution and to the countries of : Australia, Belgium, Denmark, France, Germany, Italy, Malta, Netherlands, South Africa, Spain, Sweden, Switzerland, Turkey and United Kingdom.",
      "state": "PA",
      "product_description": "Aliquot Delivery Kit (Syringe and Plunger); for use in open and percutaneous procedures to facilitate placement of bone cement in weakened or diminished bone",
      "report_date": "20150923",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Orthovita, Inc., dBA Stryker Orthobiologics.",
      "recall_number": "Z-2772-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "72054",
      "termination_date": "20170310",
      "more_code_info": "",
      "recall_initiation_date": "20150820",
      "postal_code": "19355-1302",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}