{
  "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-0817-2007",
      "event_date_initiated": "2007-04-06",
      "event_date_posted": "2007-05-22",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-03-02",
      "res_event_number": "37852",
      "product_code": "JCC",
      "product_description": "Medtronic Buffer Solution pH 1.07 500ml \nREF 9012D1071 \nManufactured by/for Medtronic A/S Tonsbakken 16-18 DK-2740 Skovlunde, Denmark",
      "code_info": "Lot #2610596",
      "firm_fei_number": "2182207",
      "recalling_firm": "Medtronic Neuromodulation",
      "address_1": "800 53rd Ave NE",
      "address_2": "PO Box 1250",
      "city": "Minneapolis",
      "state": "MN",
      "postal_code": "55440-1250",
      "additional_info_contact": "763-514-5174",
      "reason_for_recall": "Medtronic pH 1.07 buffer solution lot #2610596 was mislableled.",
      "root_cause_description": "Other",
      "action": "Customers were sent a recall notice, a customer detail sheet for this product lot, and a reply form to be used when returning the suspect bottles. Distributor was provided with a formatted templates to be used in recalling the supsect bottles from their customers and instructions on how to manage the returns and ship the bottles back to Medtronic.",
      "product_quantity": "238",
      "distribution_pattern": "Nationwide.",
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        "device_name": "Ph Buffer",
        "medical_specialty_description": "Pathology",
        "regulation_number": "864.4010",
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