{
  "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,
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  },
  "results": [
    {
      "cfres_id": "30656",
      "product_res_number": "Z-0294-04",
      "event_date_initiated": "2003-11-12",
      "event_date_posted": "2004-01-06",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-02-25",
      "res_event_number": "27864",
      "product_code": "MKI",
      "k_numbers": [
        "K012274"
      ],
      "product_description": "LIFEPAK 20 defibrillator/monitor.  Paddle sets, an optional accessory item, used with the LP 20.",
      "code_info": "Part numbers: 3200936-000, 3200936-001, 3200936-003, 3200936-010.    Date codes affected: 19680, 19681, or 19682  The firm shipped sets of paddles with shipments of devices with serial numbers listed.  However, a set of paddles was not shipped specifically with each LP 20, and a customer may receive (per order) more devices than paddle sets.  The paddles may be used with the devices specified below, or with any other LP 20 device.  LP 20 serial numbers shipped: 31481310, 31487712, 31469046, 31480240, 31488466, 31488468, 31488472, 31488479, 31488482, 31488483, 31488485, 31488486, 31488487, 31488491, 31488492, 31488494, 31488495, 31488498, 31488499, 31488500, 31488502, 31488503, 31488505, 31488970, 31488971, 31488976, 31490835, 31490862, 31490864, 31490865, 31490914, 31492668, 31494830, 31494961, 31495055, 31496204, 31496499, 31496500, 31496502, 31497170, 31497171, 31497173, 30540237, 30541490, 30524326, 31405298, 31405302, 31406327, 31406328, 31406329, 31406330, 31407066, 31420549, 31461553, 31461548, 31461559, 31461565, 31451566, 31461568, 31461569, 31461575, 31461576, 31461578, 31461580, 31461583, 31469733, 31469741, 31469747, 31481173, 31481174, 31481261, 31481265, 31481277, 31481279, 31481281, 31490863, 31490913, 31491385, 31491387, 31491390, 31491441, 31491443, 31491445, 31491384, 31491388, 31491442, 31461579, 31491444, 31494875, 31494878, 31494883, 31494884, 31490836, 31492587, 31480230, 31488975, 31494882, 31488501, 31481264, 31409217, 31481262, 31412444, 31488474, 31488470, 31481152, 31481183, 31486080, 31486083, 31488340, 31488343, 31488344, 31495057, 31495686, 31499486, 31481318, 31488973, 31491581, 31469686, 31462754, 31461567, 31461555, 31461564, 31471398, 31462757, 31461558, 31469688, 31492591, 31461574, 31480226, 31462758, 31487665, 31469037, 31469038, 31469039, 31469041, 31469043, 31469044, 31469045, 31469689, 31469690, 31480222, 31480232, 31480234, 31480238, 31469678, 31469719, 31469707, 31469727, 31461560, 31481193, 31486082, 31487666, 31461570, 31469675, 31469677, 31469680, 31469682, 31469704, 31469709, 31469714, 31481269, 31491801, 31492056, 31492128, 31469711, 31469699, 31494874, 31461551, 31493149, 31471394, 31493147, 31480235, 31461577, 31462761, 31462768, 31469670, 31481321, 31488341, 31488342, 31488481, 31488489, 31488490, 31488493, 31488497, 31488504, 31488977, 31491065, 31491580, 31491803, 31492053, 31492588, 31492589, 31492590, 31492667, 31492669, 31493144, 31493146, 31493148, 31494428, 31494430, 31494433, 31494434, 31495056, 31495058, 31495059, 31495409, 31496498, 31501828, 31501829, 31469702, 31448168, 31461573, 31469710, 31469661, 31469684, 31496197, 31481313, 31469726, 31469730, 31462762",
      "firm_fei_number": "3015876",
      "recalling_firm": "Medtronic Physio Control Corp",
      "address_1": "11811 Willows Rd NE",
      "city": "Redmond",
      "state": "WA",
      "postal_code": "98073",
      "additional_info_contact": "425-867-4000",
      "reason_for_recall": "Device unable to recognize the connection to the hard paddles accessory.",
      "root_cause_description": "Other",
      "action": "Beginning on 11/12/03 representatives from the firm visited the consignees and replaced the paddles.  A letter dated November 2003 was provided to the consignees.",
      "product_quantity": "180 sets",
      "distribution_pattern": "The firm distributed devices to 32 hospitals and medical centers located throughout the United States.",
      "openfda": {}
    }
  ]
}