{
  "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": "2026-07-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Carlsbad",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99221",
      "recalling_firm": "SEASPINE ORTHOPEDICS CORPORATION",
      "address_1": "5770 Armada Dr",
      "address_2": "N/A",
      "postal_code": "92008-4608",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "Worldwide - US Nationwide distribution including in the states of Alabama, Arizona, California, Colorado, Connecticut, Florida, Illinois, Indiana, Kansas, Maryland, Michigan, Missouri, Mississippi, Montana, Nevada, Ohio, Oklahoma, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, and Wyoming. The countries of Chile and Australia.",
      "recall_number": "Z-2762-2026",
      "product_description": "SeaSpine Polyaxial Head  REF Number: 41-3010",
      "product_quantity": "796 units",
      "reason_for_recall": "Due to manufacturing error, polyaxial  head may popoff  from the screw intraoperatively following insertion.",
      "recall_initiation_date": "20260528",
      "center_classification_date": "20260720",
      "report_date": "20260729",
      "code_info": "UDI: 10889981155117; Affected Lots: AW199682G, AW199684G."
    }
  ]
}