{
  "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,
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      "product_res_number": "Z-0111-2018",
      "event_date_initiated": "2017-09-10",
      "event_date_created": "2017-11-18",
      "recall_status": "Open, Classified",
      "res_event_number": "78125",
      "product_code": "FPK",
      "k_numbers": [
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      "product_description": "Medtronic MiniMed(TM) Pro-set(TM) (MMT-280, 281)",
      "code_info": "Lot Numbers:  6211649, 6207537",
      "firm_fei_number": "3003166194",
      "recalling_firm": "Medtronic Inc.",
      "address_1": "18000 Devonshire St",
      "city": "Northridge",
      "state": "CA",
      "postal_code": "91325-1219",
      "additional_info_contact": "Medtronic\n888-204-7616",
      "reason_for_recall": "Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.",
      "root_cause_description": "Component design/selection",
      "action": "The firm initiated its recall on 09/11/2017 by issuing a public notice, following with letters and emails.  The firm also employed the use of Facebook and Twitter as well as posting on its website.   The recall notice directs the customer to visit https://checklots.medtronicdiabetes.com for information on the lot numbers.  Persons with additional questions may call Medtronic at 1.888.204.7616.",
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