{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "115790",
      "product_res_number": "Z-0836-2013",
      "event_date_initiated": "2012-12-17",
      "event_date_posted": "2013-02-17",
      "recall_status": "Terminated",
      "event_date_terminated": "2013-12-24",
      "res_event_number": "64307",
      "product_code": "LZG",
      "k_numbers": [
        "K032257",
        "K042873"
      ],
      "product_description": "Animas(R) 2020, Animas(R) IR 1250 (1200 plus), Animas(R) IR 1200 Insulin Infusion Pumps\r\nIndicated for continuous subcutaneous infusion of insulin.",
      "code_info": "All Animas 2020, IR1250 and IR1200 Pump Models - Part Numbers 101370-00, 101371-00, 101372-00, 101374-00, 101375-00, 100380-00, 100381-00, 100382-00, 100384-00, 100385-00, 100450-00, 100210-00, 100211-00, 100212-00, 100250-00, 100251-00, 100252-00, 100200-00, 100201-00, 100202-00, 100170-00, 100171-00 and 100172-00.",
      "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": "610-644-8900",
      "reason_for_recall": "Due to an internal calendar date limit (December 31, 2015) these pumps will cease to operate on January 1, 2016, and will result in a call service alarm that is displayed on the pump display.",
      "root_cause_description": "Device Design",
      "action": "The firm initiated their recall of this product on December 17, 2012 by sending a letter to all affected customers.  The letter identified the product, problem, and actions to be taken by the customers. Contact the Animas Customer Support Department at (866) 796-6373 for questions or concerns.",
      "product_quantity": "37,998",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) including Washington, DC, Puerto Rico, US Virgin Island and the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY, and the  countries of Austria, Australia, Bermuda, Canada, New Zealand, Czech Republic, Italy, France, Finland, Hungary, Israel, United Kingdom, Spain, Sweden, Norway, Denmark, Germany, Mexico and Ireland.",
      "openfda": {
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        "fei_number": [
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        ],
        "device_name": "Pump, Infusion, Insulin",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5725",
        "device_class": "2"
      }
    }
  ]
}