{
  "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": "West Chester",
      "address_1": "1301 Goshen Pkwy",
      "reason_for_recall": "The subject product measures 4.0mm in diameter instead of 3.5mm.",
      "address_2": "",
      "product_quantity": "6",
      "code_info": "10L2702",
      "center_classification_date": "20191028",
      "distribution_pattern": "Distributed to NJ.",
      "state": "PA",
      "product_description": "Synapse System 3.5mm TI Cancellous Polyaxial Screws, Part No. 04.615.026   for use in spinal surgery",
      "report_date": "20191106",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Synthes (USA) Products LLC",
      "recall_number": "Z-0223-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83948",
      "termination_date": "20200424",
      "more_code_info": "",
      "recall_initiation_date": "20190916",
      "postal_code": "19380-5986",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}