{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Allendale",
      "state": "NJ",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65777",
      "recalling_firm": "Stryker Spine",
      "address_1": "2 Pearl Ct",
      "address_2": "N/A",
      "postal_code": "07401-1611",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution.",
      "recall_number": "Z-1976-2013",
      "product_description": "Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large 4) Large Long  5) Mini.    Allows for positioning directly on the midline keel of the occiput.",
      "product_quantity": "1536 units (US) 880 (Foreign)",
      "reason_for_recall": "Stryker has received reports from customers indicating post-operative  fracture of the pin that connects the tulip head to the plate body.",
      "recall_initiation_date": "20130530",
      "center_classification_date": "20130822",
      "termination_date": "20141230",
      "report_date": "20130828",
      "code_info": "K093670      Catalog numbers:    Small - 48551044  Medium - 48551045  Large  - 48551046  Large Long - 48551047  Mini- 48551048    All lots of the above"
    }
  ]
}