{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "35239",
      "product_res_number": "Z-0037-05",
      "event_date_initiated": "2004-09-30",
      "event_date_posted": "2004-10-22",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-11-14",
      "res_event_number": "30137",
      "product_code": "JOS",
      "k_numbers": [
        "K833364"
      ],
      "product_description": "NOVAPLUS Electrosurgical Grounding Pads, Split with Cord Catalog No. 7179V",
      "code_info": "Lot 2007-06 HP",
      "firm_fei_number": "2110898",
      "recalling_firm": "3M Company / Medical Division",
      "address_1": "3M Center, Bldg 275-05-W-06 3M Center Bldg",
      "city": "South St Paul",
      "state": "MN",
      "postal_code": "55411",
      "additional_info_contact": "Suzanne M. Danielson\n888-280-3745",
      "reason_for_recall": "Improper wire placement from the patient plate to the ESU connector plug results in an intermittent displacement connection.",
      "root_cause_description": "Other",
      "action": "A recall notification letter dated 09/30/2004 was sent to Hospitals and Health Care Distributors instructing consignees to immedately remove all effective product from lot 2007-06 HP.",
      "product_quantity": "384 cases containing 40 pads each for a total of 15,360 pads",
      "distribution_pattern": "The subject product lot was distributed to the following key 3M distributors: Owens & Minor, Cardinal Health, McKesson, Professional Health Supply, and the Burrows Company.",
      "openfda": {
        "k_number": [
          "K952290",
          "K011515",
          "K890973",
          "K873655",
          "K903302",
          "K955636",
          "K780405",
          "K923037",
          "K882421",
          "K891400",
          "K962313",
          "K012684",
          "K881144",
          "K161600",
          "K890972",
          "K993885",
          "K973554",
          "K991830",
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          "K874719",
          "K873653",
          "K050923",
          "K881763",
          "K003403",
          "K950455",
          "K000333",
          "K905060",
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          "K962544",
          "K974735",
          "K810628",
          "K952323",
          "K873654",
          "K772160",
          "K971187",
          "K792365"
        ],
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        "fei_number": [
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          "3000203000",
          "1000219637",
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          "3001451571",
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          "3007475226",
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          "3002807391",
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          "3000226659",
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          "3015136673",
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          "2020550",
          "3002808022",
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          "3010707607",
          "3014342096",
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          "1017294",
          "3002806920",
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        ],
        "device_name": "Electrode, Electrosurgical",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4400",
        "device_class": "2"
      }
    }
  ]
}