{
  "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": "2026-09-05",
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      "product_res_number": "Z-1786-2019",
      "event_date_initiated": "2019-05-03",
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      "recall_status": "Open, Classified",
      "res_event_number": "82828",
      "product_code": "NDC",
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      "firm_fei_number": "3009864844",
      "recalling_firm": "Monarch Medical Technologies",
      "address_1": "2137 South Blvd Ste 300 2137 South Blvd",
      "address_2": "Ste 300",
      "city": "Charlotte",
      "state": "NC",
      "postal_code": "28203-5189",
      "additional_info_contact": "Bruce Lisanti\n855-363-7475",
      "reason_for_recall": "Insulin dosing calculations were erroneously high.",
      "root_cause_description": "Software change control",
      "action": "The firm notified the consignees by email beginning on 05/03/2019.  The notice alerted the consignee of the problem and provided an educational brief and a tip card to provide to the staff to remind them to always use clinical judgement in following EndoTool IV dose recommendations.",
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