{
  "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": "2026-05-06",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Allendale",
      "address_1": "2 Pearl Ct",
      "reason_for_recall": "Stryker received three reports involving blades of the Luxor Retractor becoming disassembled from the base causing the retractor to collapse insitu.",
      "address_2": "",
      "product_quantity": "30 devices",
      "code_info": "Lot Code: 093309",
      "center_classification_date": "20120807",
      "distribution_pattern": "Worldwide Distribution -- US, Switzerland, Netherlands, Brazil, Hong Kong, Germany, and Taiwan.",
      "state": "NJ",
      "product_description": "LUXOR RETRACTOR BASE; Catalog Number: 48250030; Manufactured by: STRYKER Spine SAS; Z.I MARTICOT-33610-CESTAS-FRANCE; Distributed in the USA by: Stryker Spine. 2 Pearl Ct. Allendale, NJ 07401.    Provides access to the thoracic and lumbar spine from a posterior approach via a small incision.",
      "report_date": "20120815",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Spine",
      "recall_number": "Z-2155-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62648",
      "termination_date": "20131113",
      "more_code_info": "",
      "recall_initiation_date": "20120423",
      "postal_code": "07401-1611",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}