{
  "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": "48402",
      "product_res_number": "Z-0178-2007",
      "event_date_initiated": "2006-09-14",
      "event_date_posted": "2006-11-14",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-12-06",
      "res_event_number": "36313",
      "product_code": "DRM",
      "k_numbers": [
        "K972525"
      ],
      "product_description": "Michigan Instruments Thumper Mechanical CPR Device; Model 1007, Part number 15000.",
      "code_info": "All units sold in Japan (All serial numbers with 7- or 9- followed by 4 numbers; e.g. 7-xxxx or 9-xxxx).",
      "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": "Ryoji Fujisawa\n81-48-988-4411",
      "reason_for_recall": "Failure to initiate compressions when turned on.",
      "root_cause_description": "Other",
      "action": "The Japanese distributor is instructed by letter dated 9/14/06 to drill a small hole in the male checked connector at the base of the column in order to allow rapid bleed off of the pressure and to give customers a revised operators manual.",
      "product_quantity": "639",
      "distribution_pattern": "Japan.",
      "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"
      }
    }
  ]
}