{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "84024",
      "product_res_number": "Z-0208-2013",
      "event_date_initiated": "2008-08-28",
      "event_date_posted": "2012-11-06",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-11-06",
      "res_event_number": "52796",
      "product_code": "CBF",
      "k_numbers": [
        "K052713"
      ],
      "product_description": "Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model 3300E/ER\n\nThe Hyperbaric Chamber is intended to provide 100% oxygen to the patient at greater than ambient pressures.",
      "code_info": "Serial Numbers: 330001-330069, 330071, 330072, 330074, 330075.",
      "firm_fei_number": "2020676",
      "recalling_firm": "Sechrist Industries Inc",
      "address_1": "4225 E La Palma Ave",
      "city": "Anaheim",
      "state": "CA",
      "postal_code": "92807",
      "additional_info_contact": "714-579-8400",
      "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.",
      "root_cause_description": "Software design",
      "action": "Sechrist Industries contacted consignees by phone to notify them of a software upgarde and to schedule appointments to perform the required field upgrades.  An approximate summary of the phone notification is provided below.\n\"I am contacting you to notify you of a field upgrade we are performing on our\nhyperbaric chambers equipped with Electronic Control Modules in order to correct a software bug that could potentially affect the performance of your chamber. The upgrade includes the installation of a new motherboard with revised software, a reset switch, and the exchange of other control panel components. The process will take approximately 2.5 hours and will be performed at no charge to you.\"\nFor questions regarding this recall call 714-579-8400.",
      "product_quantity": "73 units",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and the countries of Bulgaria, and Canada",
      "openfda": {
        "k_number": [
          "K790693",
          "K990927",
          "K951044",
          "K081506",
          "K002794",
          "K021689",
          "K930748",
          "K993010",
          "K240569",
          "K952545",
          "K082455",
          "K001121",
          "K051759",
          "K101262",
          "K950386",
          "K002795",
          "K021693",
          "K011565",
          "K981938",
          "K220290",
          "K933929",
          "K030713",
          "K001409",
          "K832127",
          "K092991",
          "K874107",
          "K874752",
          "K072757",
          "K171899",
          "K011592",
          "K955535",
          "K842303",
          "K030418",
          "K962869",
          "K954387",
          "K011866",
          "K983648",
          "K140559",
          "K951125",
          "K060739",
          "K962871",
          "K100268",
          "K905168",
          "K031649",
          "K040145",
          "K053498",
          "K972908",
          "K022214",
          "K152223",
          "K052713",
          "K862198",
          "K861315",
          "K021690",
          "K960389",
          "K850563",
          "K041007",
          "K052866",
          "K010659",
          "K072427",
          "K020974",
          "K974868",
          "K841608",
          "K950957",
          "K840841",
          "K934164",
          "K984313",
          "K163109",
          "K011312",
          "K102831"
        ],
        "registration_number": [
          "3004035771",
          "3007127387",
          "3010317211",
          "3013938915",
          "1000402893",
          "1036464",
          "3016489995",
          "2438426",
          "8043539",
          "3005505220",
          "3013976593",
          "3006777109",
          "1000519737",
          "3007319244",
          "2020676",
          "3016467917",
          "3006097795",
          "3013595329"
        ],
        "fei_number": [
          "3004035771",
          "3007127387",
          "3010317211",
          "3013938915",
          "1000402893",
          "1036464",
          "1000624398",
          "1037230",
          "3016489995",
          "3005505220",
          "3010251686",
          "3006777109",
          "1000519737",
          "3007319244",
          "2020676",
          "3016467917",
          "3006097795",
          "3013595329"
        ],
        "device_name": "Chamber, Hyperbaric",
        "medical_specialty_description": "Anesthesiology",
        "regulation_number": "868.5470",
        "device_class": "2"
      }
    }
  ]
}