{
  "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": "73523",
      "product_res_number": "Z-0290-2009",
      "event_date_initiated": "2008-08-04",
      "event_date_posted": "2008-11-25",
      "recall_status": "Terminated",
      "event_date_terminated": "2010-02-04",
      "res_event_number": "49476",
      "product_code": "LZG",
      "k_numbers": [
        "K080639"
      ],
      "product_description": "Battery Caps used with insulin pumps and glucose monitoring systems.  \n\nThe pump is used to help maintain blood glucose targets.",
      "code_info": "Part Number:  100-158-01.  All units (no serial numbers).",
      "firm_fei_number": "3002920072",
      "recalling_firm": "Animas Corporation",
      "address_1": "200 Lawrence Dr",
      "city": "West Chester",
      "state": "PA",
      "postal_code": "19380",
      "additional_info_contact": "Consumer Relations\n866-423-4087",
      "reason_for_recall": "Unintentional rebooting: Pump products exhibit an intermittent loss of power due intermittent loss of contact between battery cap and battery canister resulting in the device resetting.  The failure of the battery cap may result in failure of the device to administer insulin therapy which may result in hyperglycemia.",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "The recalling firm issued a notification letter to the patients with insulin pumps on 8/5/08 to inform them of the problem and that they needed to replace the battery. The recalling firm contacted OneTouch Ping users by telephone on 8/5/08 for this issue and another issue. The recalling firm issued letters to distributors informing them of the problem and notified customers to replace the batteries. In addition, a letter was issued to physicians to alert them of the situation with regard to current patients.  Consumers can contact 1-800-423-4087 for additional information or questions.",
      "product_quantity": "1,388 caps",
      "distribution_pattern": "Worldwide Distribution including USA (AR, CA, FL, KY, LA, MA, NE, OH, PA, SC, SD, TN, and UT) and countries of Australia, Austria, Canada, Czech Republic, Finland, France, Israel, Italy, New Zealand, Spain, Switzerland, and Sweden.",
      "openfda": {
        "k_number": [
          "K022317",
          "K042792",
          "K013807",
          "K043000",
          "K160482",
          "K160056",
          "K900498",
          "K021439",
          "K223372",
          "K994186",
          "K093364",
          "K991376",
          "K142619",
          "K041317",
          "K100567",
          "K031738",
          "K042873",
          "K141758",
          "K082595",
          "K905693",
          "K062323",
          "K030531",
          "K133593",
          "K041318",
          "K071788",
          "K022394",
          "K071613",
          "K960001",
          "K103825",
          "K032164",
          "K063126",
          "K162296",
          "K031373",
          "K100504",
          "K180045",
          "K160252",
          "K050312",
          "K082590",
          "K022831",
          "K192659",
          "K023471",
          "K111353",
          "K143189",
          "K211575",
          "K131294",
          "K993012",
          "K032257",
          "K050760",
          "K182630",
          "K053177",
          "K080639",
          "K073356",
          "K210714",
          "K253534",
          "K901588",
          "K111210",
          "K083225",
          "K884978",
          "K040676",
          "K963948",
          "K162080",
          "K042887",
          "K031541",
          "K001604",
          "K090245",
          "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",
          "9616814",
          "1313700",
          "3012421607",
          "3008824097",
          "2029275",
          "3006479639",
          "3020976354",
          "3010162782",
          "3007007790",
          "3007981285",
          "3005627859",
          "9610126",
          "3013636348",
          "2246552",
          "3010047442",
          "3007710663",
          "3014585508",
          "1721676",
          "3009337401",
          "3006194679",
          "3001058982",
          "9617604",
          "3016540876",
          "3015218509",
          "1220477",
          "3008810357",
          "3010291427",
          "3011393376",
          "3002806818",
          "2032227",
          "3007939342",
          "3007871880",
          "3013756811"
        ],
        "fei_number": [
          "3009515470",
          "3002806559",
          "3005340341",
          "3027453514",
          "3042027705",
          "1313700",
          "3003166194",
          "3002558692",
          "3012421607",
          "3008824097",
          "3006479639",
          "3004173703",
          "3020976354",
          "1000306431",
          "3010162782",
          "3007007790",
          "3007981285",
          "3005627859",
          "3013636348",
          "2246552",
          "3010047442",
          "3014585508",
          "1721676",
          "3009337401",
          "3006194679",
          "3003024060",
          "3001058982",
          "3016540876",
          "3015218509",
          "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"
      }
    }
  ]
}