{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "65564",
      "product_res_number": "Z-0529-2008",
      "event_date_initiated": "2007-10-19",
      "event_date_posted": "2008-01-23",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-04-25",
      "res_event_number": "45482",
      "product_code": "NFB",
      "k_numbers": [
        "K051988"
      ],
      "product_description": "Oxy Serve II Oxygen Conserving Regulator, Model Number: MCRB-870-6, Superior Products, Inc/SP Medical, LLC, Cleveland, Ohio 44144",
      "code_info": "Lot 051101 -  (Serial #'s: 001009, 001010, 001012, 001017, 001019, 001023, 001025, 001027, & 001029) -- Lot 05111 - (Serial #: 001049)--  Lot 051121 (Serial #'s: 001022, 001015, 001026, 530002, 530004, 001013, 001014, 001016, & 001034)--  Lot 051130 (Serial #'s: 530003, 001011, 001018, 001021, 001024, 001031, 001033, 001035, 001037, 001038, 001039, & 001050) -- Lot 051202 (Serial # 001044)-- Lot 063759 (Serial #'s: 001206, 001054, 001055, 001056, 001073, 001077, 001164, 001168, 001180, 001191, 001207, 001078, 001166, 001154, 001178, 001169, 001170, 001174, 001153, 001155, 001157, 001171, 001175, 001177, 001182, 001200, 001203, 001208, 001140, & 001165) Lot 063426 (Serial # 001093, 001101, 001111, 001128, 001106, 001114, 001076, 001112, 001074, 001084, 001092, 001124, 001126, 001134, 001137, 001141, 001142, 001167, 001069, 001057, 001099, 001130, 001135, 001150, 001118, 001139, 001075, 001052, 001117, 001119, 001176, 001061, 001053, 001103, 0011363, 001108, 001067, 001110, 001070, 001136, 001098, 001121, 001113, 001051, 001063, 001082, 001071, 001116, 001064, 001066, 001095, 001109, 001085, 001087, 001088, 001089, 001090, 001091, 001094, 001096, 001125, 001127, 001144, & 001145)",
      "firm_fei_number": "1000515374",
      "recalling_firm": "Superior Products Inc",
      "address_1": "3786 Ridge Rd",
      "city": "Cleveland",
      "state": "OH",
      "postal_code": "44144-1127",
      "additional_info_contact": "216-651-9400 Ext. 144",
      "reason_for_recall": "Leakage: Device was leaking oxygen",
      "root_cause_description": "Component design/selection",
      "action": "A Voluntary Medical Device Recall notification was  delivered by certified mail on or about 10/19/2007, to all consignee's; \"bill to\" and \"sent to.\"  Consignee's are asked to contact their customers (if any), notify them of the recall, and return all implicated products to Superior Products.",
      "product_quantity": "125",
      "distribution_pattern": "Worldwide-USA including states of  CA, FL, IA, IN, KY, OH, SC, TX, and  WA. and countries of Singapore, Mexico City, MX, and Turkey",
      "openfda": {
        "k_number": [
          "K221014",
          "K023420",
          "K852650",
          "K250322",
          "K884754",
          "K060382",
          "K963247",
          "K853378",
          "K883590",
          "K051988",
          "K982943",
          "K113111",
          "K861199",
          "K953852",
          "K010389",
          "K131023",
          "K010747",
          "K070740",
          "K001412",
          "K964541",
          "K903504",
          "K042142",
          "K151506",
          "K923660",
          "K962944",
          "K883216",
          "K041568",
          "K000890",
          "K863695",
          "K890141",
          "K060751",
          "K051007",
          "K020475",
          "K962766",
          "K020329",
          "K884562",
          "K002284",
          "K892407",
          "K200401",
          "K033197",
          "K031983",
          "K001579",
          "K033364",
          "K874804",
          "K890298",
          "K864127",
          "K992659",
          "K961126",
          "K032018",
          "K003455",
          "K983601",
          "K990678",
          "K873901",
          "K090421",
          "K024023",
          "K220591",
          "K992935",
          "K830009",
          "K023673",
          "K022865",
          "K861325",
          "K983459",
          "K103392",
          "K955129",
          "K052563",
          "K834588",
          "K851235",
          "K892639",
          "K970371",
          "K051540",
          "K041057"
        ],
        "registration_number": [
          "3009128734",
          "1000604079",
          "8030673",
          "3004748541",
          "3004050971",
          "3013557562",
          "3017865349",
          "1062191",
          "3005380088",
          "3008776780",
          "1924066",
          "3012494290",
          "3012316249",
          "3010272829",
          "2523148",
          "1314417",
          "3004972304"
        ],
        "fei_number": [
          "1000604079",
          "3000719543",
          "3004748541",
          "3004050971",
          "2523148",
          "3013557562",
          "3017865349",
          "3005380088",
          "1924066",
          "3008776780",
          "3012494290",
          "3012316249",
          "3010272829",
          "2129616",
          "1314417",
          "3004213967",
          "3004972304"
        ],
        "device_name": "Conserver, Oxygen",
        "medical_specialty_description": "Anesthesiology",
        "regulation_number": "868.5905",
        "device_class": "2"
      }
    }
  ]
}