{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Billerica",
      "state": "MA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71651",
      "recalling_firm": "Insulet Corporation",
      "address_1": "600 Technology Park Dr Ste 200",
      "address_2": "N/A",
      "postal_code": "01821-4126",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide Distribution: US (Nationwide) and country of: Switzerland.",
      "recall_number": "Z-2485-2015",
      "product_description": "OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected.  Catalog Number(s): 14810 (OUS).  Intended for subcutaneous delivery of insulin at set and variable rates for the management of diabetes mellitus in persons requiring insulin.",
      "product_quantity": "16,017 boxes. Expanded Recall: 5,179.0 boxes",
      "reason_for_recall": "OmniPods¿ (Pods) have a higher rate of failure causing:  Cannula fails to deploy/retract causing insulin to be pumped or the audible alarm is displayed on the PDM and pod will not deliver insulin",
      "recall_initiation_date": "20150713",
      "center_classification_date": "20150904",
      "termination_date": "20170126",
      "report_date": "20150916",
      "code_info": "Lot Numbers:  L40771, L40892, L40901,  L40905, L40997, L41199,  L41208    Expanded Recall:  Lot Codes: L41908, L41910, F41935"
    }
  ]
}