{
  "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": "Anaheim",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "52796",
      "recalling_firm": "Sechrist Industries Inc",
      "address_1": "4225 E La Palma Ave",
      "address_2": "N/A",
      "postal_code": "92807",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and the countries of Bulgaria, and Canada",
      "recall_number": "Z-0208-2013",
      "product_description": "Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model 3300E/ER    The Hyperbaric Chamber is intended to provide 100% oxygen to the patient at greater than ambient pressures.",
      "product_quantity": "73 units",
      "reason_for_recall": "Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with Electronic Control Modules in order to correct a software bug that could potentially affect the performance of the chamber.",
      "recall_initiation_date": "20080828",
      "center_classification_date": "20121106",
      "termination_date": "20121106",
      "report_date": "20121114",
      "code_info": "Serial Numbers: 330001-330069, 330071, 330072, 330074, 330075."
    }
  ]
}