{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "149271",
      "product_res_number": "Z-0329-2017",
      "event_date_initiated": "2016-08-24",
      "event_date_created": "2016-11-02",
      "recall_status": "Terminated",
      "event_date_terminated": "2017-10-06",
      "res_event_number": "75066",
      "product_code": "MRV",
      "k_numbers": [
        "K042183"
      ],
      "product_description": "Glucose Tolerance Beverage- Orange 50 gram Concentration, Liquid 4/Pack of 6 bottles, 24/case\nAccessory  to an In Vitro Diagnostic Oral Glucose Tolerance Test (OGTT) in the evaluation of diabetes mellitus and related disease conditions. Oral Glucose Tolerance Drinks provide a premeasured glucose load of either 50 grams, 75 grams or 100 grams. After the glucose load is consumed, measurements of blood glucose are drawn at specific time intervals to determine potential defects in insulin secretion and/or insulin action. Insulin is the hormone produced by the pancreas that moves glucose from the bloodstream into cells. 50 gram glucose loads are typically administered for the initial screening of gestational diabetes. 75 gram glucose loads are typically administered for the diagnosis of diabetes mellitus. 100 gram glucose loads are typically administered for the diagnosis of gestational diabetes.",
      "code_info": "Item Number: 10-O-050 Lot Number: 51426 Expiration Date: 05/2018",
      "firm_fei_number": "3009963993",
      "recalling_firm": "Azer Scientific, Inc.",
      "address_1": "701 Hemlock Rd",
      "city": "Morgantown",
      "state": "PA",
      "postal_code": "19543-9768",
      "reason_for_recall": "Out of Specification Microbiological test results",
      "root_cause_description": "Unknown/Undetermined by firm",
      "action": "Azer Scientific mailed an Urgent Medical Device Recall letter dated August 30, 2016, to all affected customers.  The letter identified the product, the problem, and the action to be taken by the customer.  Customers were asked to discontinue use of product and discard to avoid further distribution or use and to notify their customers/end users of the recall.  Customers were asked to acknowledge receipt of the letter by completing the attached form and faxing it to (610) 901-3046.  Customers with questions were instructed to call (610) 524-5810.",
      "product_quantity": "426 cases",
      "distribution_pattern": "Nationwide Distribution",
      "openfda": {
        "k_number": [
          "K120247",
          "K032753",
          "K042183"
        ],
        "registration_number": [
          "3009963993",
          "3006349554",
          "1181121",
          "1417592",
          "2226984",
          "2513595",
          "3017544399"
        ],
        "fei_number": [
          "3009963993",
          "3006349554",
          "1181121",
          "1417592",
          "2226984",
          "2513595",
          "3017544399"
        ],
        "device_name": "Drink, Glucose Tolerance",
        "medical_specialty_description": "Clinical Chemistry",
        "regulation_number": "862.1345",
        "device_class": "2"
      }
    }
  ]
}