{
  "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": "161387",
      "product_res_number": "Z-0703-2018",
      "event_date_initiated": "2017-07-31",
      "event_date_posted": "2018-02-23",
      "recall_status": "Terminated",
      "event_date_terminated": "2019-03-29",
      "res_event_number": "79107",
      "product_code": "IXR",
      "product_description": "Foot Controls impacted for the following devices:\n\nOAKWORKS Medical CFPM 300 Imaging Table\nOAKWORKS Medical CFPM 301 Imaging Table\nOAKWORKS Medical CFPM 400 Imaging Table\nOAKWORKS Medical CFPM 401 Imaging Table\nOAKWORKS Medical CFPMB 301 Bariatric Imaging Table\nOAKWORKS Medical CFUR 301 Urology Table\nOAKWORKS Medical CFUR 401 Urology Table\nOAKWORKS Medical CFLU 401 Lithotripsy/Urology Table",
      "code_info": "MODEL #(s):  \"CFPM 300 \"CFPM 301  \"CFPM 400 \"CFPM 401  \"CFPMB 301 \"CFUR 301 \"CFUR 401 \"CFLU 401  CATALOG #(s): \"75208-T01 and 75209-T01 \"75211-T01 and 75212-T01  \"75204-T01 and 75205-T01 \"75206-T01 and 75207-T01 \"75213-T01 \"75214-T01 \"75215-T01 \"75216-T01",
      "firm_fei_number": "1000121370",
      "recalling_firm": "Oakworks Inc",
      "address_1": "923 E Wellspring Rd",
      "city": "New Freedom",
      "state": "PA",
      "postal_code": "17349-8408",
      "additional_info_contact": "Deborah Berg\n717-759-3118",
      "reason_for_recall": "The foot control used on the OAKWORKS Inc., CFPM300, CFPM301, CFPM400, CFPM401, CFPMB301, CFUR301, CFUR401 and CFLU401 Imaging Tables can become lodged under the base or under the column of the table.",
      "root_cause_description": "Device Design",
      "action": "OAKWORKS,  Inc. issued a MEDICAL DEVICE ADVISORY NOTICE dated 8/18/2017 to customers providing more information in regards to the Medical Device Advisory Notice sent on May 12, 2017.  The advisory notice was initiated in response to reported issues with the foot control.  OakWorks, Inc. customer service will place the order for the appropriate Foot Control Kit listed below based on what table is impacted and the date of manufacture. \n\nPN\n2015-204   - Foot Control Kit - Standard Riser\n2015-209   - Foot Control Kit - Thinner Riser\n2015-210   - Foot Control Kit - Holder Only\n2015-211   - Foot Control Kit - Riser Removal\n\nCustomers with questions may contact 1-800-558-8850 or 1-717-235-6807.",
      "product_quantity": "1,104",
      "distribution_pattern": "USA (nationwide) Distribution",
      "openfda": {
        "k_number": [
          "K950402",
          "K912996",
          "K843926",
          "K911267",
          "K874114",
          "K771293",
          "K905152",
          "K883162",
          "K931563",
          "K943581",
          "K922364",
          "K954356",
          "K883153",
          "K792326",
          "K924326",
          "K920728",
          "K915853",
          "K912741",
          "K965096",
          "K874113",
          "K934574",
          "K840226",
          "K760466",
          "K945842",
          "K883863",
          "K944987",
          "K920742",
          "K965105",
          "K770334",
          "K903422",
          "K792645",
          "K896583",
          "K903395",
          "K870707",
          "K901654",
          "K940721",
          "K920726",
          "K896324",
          "K961022",
          "K912586",
          "K951176",
          "K914417",
          "K854478",
          "K854486",
          "K905153",
          "K860913",
          "K893673",
          "K953557",
          "K781532",
          "K920722",
          "K914165",
          "K850948",
          "K892226",
          "K925175",
          "K840227",
          "K971128",
          "K853175",
          "K905501",
          "K854085",
          "K910838",
          "K905265",
          "K791812",
          "K963851",
          "K911098",
          "K913147",
          "K973039",
          "K880529",
          "K882019",
          "K902989",
          "K970640",
          "K935444",
          "K884531",
          "K953556",
          "K000412",
          "K896119",
          "K950981",
          "K922591"
        ],
        "registration_number": [
          "8022065",
          "3033525986",
          "3002808176",
          "9610903",
          "3013846070",
          "3033527770",
          "3000126629",
          "1223864",
          "8030233",
          "9616014",
          "1225473",
          "3007912863",
          "3003927316",
          "3003768251",
          "3012010520",
          "9613445",
          "3010496070",
          "3004977335",
          "3015276088",
          "3008284470",
          "3009077524",
          "2243057",
          "2529571"
        ],
        "fei_number": [
          "3033525986",
          "3002808176",
          "3013846070",
          "3033527770",
          "1000121370",
          "3000126629",
          "3002807145",
          "3002675731",
          "3007912863",
          "3003927316",
          "3002808139",
          "3003768251",
          "3012010520",
          "1000305755",
          "3001237319",
          "3003434037",
          "3002175190",
          "3010496070",
          "3004977335",
          "3015276088",
          "3008284470",
          "3009077524",
          "2243057"
        ],
        "device_name": "Table, Radiographic, Tilting",
        "medical_specialty_description": "Radiology",
        "regulation_number": "892.1980",
        "device_class": "2"
      }
    }
  ]
}