{
  "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": {
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      "product_res_number": "Z-0347-2020",
      "event_date_initiated": "2018-12-18",
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      "recall_status": "Terminated",
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      "res_event_number": "82003",
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      "code_info": "Lot Numbers L000120, L000121, L000122, L000123, L000124, L000131, L000132, L000133, L000135, L000136",
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      "recalling_firm": "Insulet Corporation",
      "address_1": "600 Technology Park Dr Ste 200 600 Technology Park Dr",
      "address_2": "Ste 200",
      "city": "Billerica",
      "state": "MA",
      "postal_code": "01821-4150",
      "reason_for_recall": "There is a potential for a communication interruption following a bolus command that may result in inaccurate information presented in insulin on board (IOB), last bolus field or bolus history.",
      "root_cause_description": "Software design",
      "action": "Urgent Medical Device Correction letters dated 12/18/18 were sent to customers.",
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