{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "West Chester",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70055",
      "recalling_firm": "Synthes, Inc.",
      "address_1": "1302 Wrights Ln E",
      "address_2": "N/A",
      "postal_code": "19380-3417",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Distributed in the state of WI",
      "recall_number": "Z-1094-2015",
      "product_description": "Hemostatic Bone Putty,  for use as a water-soluble implant material and for use in the control of bleeding from bone surfaces.",
      "product_quantity": "38",
      "reason_for_recall": "Revision A of the Hemostatic Bone Putty Brochure (J10847A) was sent to sales consultants instead of Revision B (J10847B), which corrected an error in the indication statement.",
      "recall_initiation_date": "20120106",
      "center_classification_date": "20150211",
      "termination_date": "20150330",
      "report_date": "20150218",
      "code_info": "Part 10847A"
    }
  ]
}