{
  "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": {
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  "results": [
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      "status": "Terminated",
      "city": "West Chester",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76182",
      "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": "United States Nationwide Distribution.",
      "recall_number": "Z-1124-2017",
      "product_description": "Synthes Radial Head Prosthesis System, Surgical instrument motors and accessories    Product Usage:  Intended for primary and revision joint replacement of the radial head.",
      "product_quantity": "50,311 units",
      "reason_for_recall": "There is the possibility that the radial stem may loosen post-operatively at the stem bone interface.",
      "recall_initiation_date": "20161229",
      "center_classification_date": "20170202",
      "termination_date": "20180206",
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