{
  "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": "41703",
      "product_res_number": "Z-0116-06",
      "event_date_initiated": "2005-09-02",
      "event_date_posted": "2005-11-02",
      "recall_status": "Terminated",
      "event_date_terminated": "2011-01-17",
      "res_event_number": "33327",
      "product_code": "LDD",
      "k_numbers": [
        "K012274"
      ],
      "product_description": "QUIK-COMBO pacing/defibrillation/ECG (therapy) cables used with the LIFEPAK 12 defibrillator/monitor series.",
      "code_info": "Cables do not contain serial numbers. Therapy cable part number: 3006570-006 and below",
      "firm_fei_number": "3015876",
      "recalling_firm": "Medtronic Emergency Response Systems, Inc.",
      "address_1": "11811 Willows Rd Ne",
      "city": "Redmond",
      "state": "WA",
      "postal_code": "98052-2003",
      "additional_info_contact": "John A. Parks\n425-867-4681",
      "reason_for_recall": "Potential for voltage pins in connector of therapy cable to break.",
      "root_cause_description": "Other",
      "action": "On 9/2/05 the firm issued letters dated September 2005 to their customers. The letters state the problem, advise the cables and/or connectors will be replaced, and emphasize daily inspection and testing,",
      "product_quantity": "total for both types - 52,654",
      "distribution_pattern": "Devices were distributed worldwide.",
      "openfda": {
        "k_number": [
          "K962551",
          "K801544",
          "K931787",
          "K780416",
          "K800936",
          "K852799",
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          "K912966",
          "K103159",
          "K842667",
          "K904462",
          "K140502",
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          "K935111",
          "K813471",
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          "K842312",
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          "K910144",
          "K851092",
          "K874697",
          "K911662",
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          "K982896",
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          "K913484",
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          "K811638",
          "K921487",
          "K822294",
          "K882235",
          "K894355",
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          "K971436",
          "K872793",
          "K921606",
          "K855082",
          "K012274",
          "K934508",
          "K842624",
          "K851485",
          "K103651",
          "K914971",
          "K911604",
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          "K935674",
          "K800937",
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          "K203231",
          "K921765",
          "K931803",
          "K851931",
          "K963781",
          "K854307",
          "K902478",
          "K923864",
          "K952085",
          "K941995",
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          "K842235",
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          "K910754",
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          "K903657",
          "K833751",
          "K890079",
          "K935083",
          "K931804",
          "K812520",
          "K880575",
          "K904466",
          "K894356",
          "K852808",
          "K832833",
          "K900169",
          "K922172",
          "K970481",
          "K912587",
          "K895533",
          "K822961",
          "K822617",
          "K103334",
          "K863303",
          "K902288",
          "K881153",
          "K812317",
          "K030417",
          "K931266",
          "K840246",
          "K934015",
          "K895009",
          "K182503",
          "K011461",
          "K840900",
          "K832827",
          "K823828",
          "K831696",
          "K891122",
          "K812586",
          "K781678",
          "K840167",
          "K851924",
          "K911665",
          "K874091",
          "K844740",
          "K874204",
          "K902782",
          "K863405",
          "K863899",
          "K940842",
          "K871135",
          "K843396",
          "K912621",
          "K864257",
          "K920990",
          "K902429",
          "K852905",
          "K895662"
        ],
        "registration_number": [
          "3007029079",
          "1220908",
          "3010783192",
          "3003800159",
          "3010703925",
          "3017422354",
          "3015997711",
          "2183890",
          "3004035727",
          "3005521864",
          "1317188",
          "3012104670",
          "1417592",
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          "1320894",
          "3003832357",
          "3013557562",
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          "3014579161",
          "3015876"
        ],
        "fei_number": [
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          "3000957797",
          "3003832357",
          "3013557562",
          "3014579161",
          "1000524572",
          "3001451571",
          "3015876"
        ],
        "device_name": "Dc-Defibrillator, Low-Energy, (Including Paddles)",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.5300",
        "device_class": "2"
      }
    }
  ]
}