{
  "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": "47197",
      "product_res_number": "Z-0119-2007",
      "event_date_initiated": "2006-08-04",
      "event_date_posted": "2006-11-03",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-12-06",
      "res_event_number": "35934",
      "product_code": "DRM",
      "k_numbers": [
        "K972525"
      ],
      "product_description": "Michigan Instruments Thumper Mechanical CPR Device; Model 1007.",
      "code_info": "All units with a manual configuration (as opposed to a pneumatic configuration).",
      "firm_fei_number": "1821850",
      "recalling_firm": "Michigan  Instruments, Inc.",
      "address_1": "4717 Talon Court S.E.",
      "city": "Grand Rapids",
      "state": "MI",
      "postal_code": "49512-5408",
      "additional_info_contact": "800-530-9939 Ext. 312",
      "reason_for_recall": "Failure to initiate compressions when first turned on, if improperly shut down-Operator Manual updated to include proper shut down procedures",
      "root_cause_description": "Other",
      "action": "Consignees were sent a letter dated 8/4/06 with additional instructions for use.  A second letter was sent on 9/1/06 to correct the new instructions provided in the first letter for page 19 of the instructions.",
      "product_quantity": "1100",
      "distribution_pattern": "Worldwide- USA and countries of  Brazil, Canada, China, Germany, Greece, Japan, Korea, Macau, Netherlands, Pakistan, Spain, Taiwan and United Kingdom.",
      "openfda": {
        "k_number": [
          "K153628",
          "K173553",
          "K841275",
          "K841822",
          "K841410",
          "K871271",
          "K032852",
          "K112998",
          "K062401",
          "K811987",
          "K855004",
          "K161768",
          "K090422",
          "K063602",
          "K072527",
          "K791145",
          "K851139",
          "K221700",
          "K854734",
          "K790513",
          "K972525",
          "K922093",
          "K062119",
          "K801945",
          "K871272",
          "K761194",
          "K951124",
          "K792451",
          "K792454",
          "K011046",
          "K801947",
          "K811909",
          "K211289",
          "K833879",
          "K792458",
          "K962237",
          "K053403",
          "K073079",
          "K141809",
          "K022345",
          "K040453",
          "K024215",
          "K792452",
          "K102068",
          "K801946"
        ],
        "registration_number": [
          "3029871637",
          "3015876",
          "3013964848",
          "3007275459",
          "3010703925",
          "3012972516",
          "3005445717",
          "3008727520",
          "3003521780",
          "3026976873",
          "3010030355",
          "3010617000",
          "1821850"
        ],
        "fei_number": [
          "3029871637",
          "3015876",
          "3013964848",
          "3007275459",
          "3010703925",
          "3012972516",
          "3005445717",
          "3008727520",
          "3003521780",
          "3026976873",
          "3010030355",
          "3003793491",
          "1821850"
        ],
        "device_name": "Compressor, Cardiac, External",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.5200",
        "device_class": "2"
      }
    }
  ]
}