{
  "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": "35296",
      "product_res_number": "Z-0211-05",
      "event_date_initiated": "2004-09-28",
      "event_date_posted": "2004-11-19",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-03-10",
      "res_event_number": "30166",
      "product_code": "LZG",
      "k_numbers": [
        "K032257"
      ],
      "product_description": "IR 1200 Insulin Pump. IPX8 Rx only. Label P/N 400-125-00 Revision C.",
      "code_info": "Model IR 1200",
      "firm_fei_number": "3002920072",
      "recalling_firm": "Animas Corporation",
      "address_1": "200 Lawrence Dr",
      "city": "West Chester",
      "state": "PA",
      "postal_code": "19380-3428",
      "additional_info_contact": "Doug Woodruff\n610-644-8990 Ext. 1185",
      "reason_for_recall": "Suspend mode not functioning properly",
      "root_cause_description": "Other",
      "action": "The recalling firm issued a notice entitled 'Important Safety Information Regarding the Animas IR 1200 Pump' dated 9/28/04 to the health care professionals and distributors. The letter informed the reader of the problem and to use an alternate feature. Health care professionals should notify patients of the problem.",
      "product_quantity": "7395 units",
      "distribution_pattern": "The products are shipped to diabetic supply companies in FK, NE, NV, NJ, NY, OH, OK, TX, VA, and WA then further shipped to patients nationwide. The products were shipped to government accounts in IL, MD, and SC. The product was also shipped to a supply company in Israel.",
      "openfda": {
        "k_number": [
          "K022317",
          "K042792",
          "K013807",
          "K043000",
          "K160482",
          "K160056",
          "K900498",
          "K021439",
          "K223372",
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          "K093364",
          "K991376",
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          "K031738",
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          "K082595",
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          "K062323",
          "K030531",
          "K133593",
          "K041318",
          "K071788",
          "K022394",
          "K071613",
          "K960001",
          "K103825",
          "K032164",
          "K063126",
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          "K042887",
          "K031541",
          "K001604",
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          "K070844",
          "K140439",
          "K120206",
          "K973044",
          "K240158",
          "K993184",
          "K122483",
          "K051041",
          "K020655",
          "K050971",
          "K013309",
          "K990801",
          "K060876",
          "K111669",
          "K021725",
          "K972107",
          "K122953",
          "K063674",
          "K241622"
        ],
        "registration_number": [
          "3009515470",
          "3005340341",
          "3027453514",
          "3042027705",
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          "3010291427",
          "3011393376",
          "3002806818",
          "2032227",
          "3007939342",
          "3007871880",
          "3013756811"
        ],
        "fei_number": [
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          "3002806559",
          "3005340341",
          "3027453514",
          "3042027705",
          "1313700",
          "3003166194",
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          "3020976354",
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          "3010162782",
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          "3007981285",
          "3005627859",
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          "2246552",
          "3010047442",
          "3014585508",
          "1721676",
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          "3003024060",
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          "1220477",
          "3008810357",
          "3010291427",
          "3011393376",
          "3002806818",
          "3007939342",
          "3007871880",
          "3013756811"
        ],
        "device_name": "Pump, Infusion, Insulin",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5725",
        "device_class": "2"
      }
    }
  ]
}