{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Reno",
      "state": "NV",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86352",
      "recalling_firm": "Ansell Healthcare Products LLC",
      "address_1": "2301 Robb Dr",
      "address_2": "N/A",
      "postal_code": "89523-1901",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide distribution including in the states of IL, OK, WI, PA, TX, OH, MI, IN, VA, AR, KS, MO, NV, OR, FL, QC, NJ, NE, KY, AL, TN, LA, NY, SC, MS, MD, CA, GA, SD.",
      "recall_number": "Z-0051-2021",
      "product_description": "MICROFLEX Diamond Grip Examination Gloves, MF-300 - Product Usage: A patient examination glove is a disposable device intended for medical purposes that is worn on the examiner s hand or finger to prevent contamination between patient and examiner.",
      "product_quantity": "1312 Cases",
      "reason_for_recall": "Examination gloves were shipped inadvertently, without to verify barrier integrity.",
      "recall_initiation_date": "20200819",
      "center_classification_date": "20201002",
      "termination_date": "20211103",
      "report_date": "20201014",
      "code_info": "Lot: 2003LG, Batch: 20035314LG"
    }
  ]
}