{
  "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": "Sparks",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83406",
      "recalling_firm": "Becton Dickinson & Co.",
      "address_1": "7 Loveton Cir",
      "address_2": "N/A",
      "postal_code": "21152-9212",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "AL, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MT, NC, NH, NJ, NM, NV, NY, OH, OR, PA, PR, RI, SC, TN, TX, VA, WA, WI, WV    Worldwide: Australia, Belgium, Brazil, Canada, Chile, China, Hong Kong, Japan, Korea, Mexico, Singapore, Taiwan",
      "recall_number": "Z-2329-2019",
      "product_description": "Kit BD Max Enteric Parasite Panel EU;  Catalog # 442960",
      "product_quantity": "355 units",
      "reason_for_recall": "The foil bags containing extraction tubes for BD MAX\" Reagent products may not been sealed properly.",
      "recall_initiation_date": "20190717",
      "center_classification_date": "20190822",
      "termination_date": "20200513",
      "report_date": "20190828",
      "code_info": "Lot # 9106889; UDI (GTIN, DI+PI):(01)00382904429607 (17)201115(10)9106889(30)1; Exp: 11/15/2020"
    }
  ]
}