{
  "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": "2026-04-01",
    "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": "83991",
      "recalling_firm": "Synthes (USA) Products LLC",
      "address_1": "1301 Goshen Pkwy",
      "address_2": "N/A",
      "postal_code": "19380-5986",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "AR",
      "recall_number": "Z-0349-2020",
      "product_description": "MODIFIED INSTRUMENTS:  Trial Spacer 7mm with T-Handle  Trial Spacer 8mm with T-Handle  Trial Spacer 9mm with T-Handle  Trial Spacer 10mm with T-Handle  Trial Spacer 11mm with T-Handle  Trial Spacer 12mm with T-Handle  Trial Spacer 13mm with T-Handle  Trial Spacer 15mm with T-Handle  Trial Spacer 17mm with T-Handle",
      "product_quantity": "9 units",
      "reason_for_recall": "Modified outside of approved manufacturing process",
      "recall_initiation_date": "20190905",
      "center_classification_date": "20191108",
      "termination_date": "20200623",
      "report_date": "20191120",
      "code_info": "Unknown"
    }
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}