{
  "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": [
    {
      "status": "Terminated",
      "city": "West Chester",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76487",
      "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": "Letter",
      "distribution_pattern": "US distribution to TX and LA",
      "recall_number": "Z-1383-2017",
      "product_description": "PRODISC Orthopedic Manual Surgical Instrument, strut used in spinal surgery.   Part numbers 03.820.350 and 03.820.352.  Used to hold the disc segment open and facilitate discectomy",
      "product_quantity": "2 units",
      "reason_for_recall": "These items are incorrectly etched and labeled.  The item etched and labeled as 10mm Strut 03.820.350 lot 5919005 is a 12 mm Strut.  The item etched and labeled as 12 mm Strut 03.820.352 lot 5919006 is a 10 mm Strut.",
      "recall_initiation_date": "20170131",
      "center_classification_date": "20170228",
      "termination_date": "20171201",
      "report_date": "20170308",
      "code_info": "Part numbers 03.820.350 Lot 5919005 and 03.820.352, lot 5919006",
      "more_code_info": ""
    }
  ]
}