{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Sparks",
      "address_1": "BD Diagnostic Systems",
      "reason_for_recall": "In-vitro diagnostic agents were placed into incorrect packaging for distribution to microbiological laboratories.",
      "address_2": "7 Loveton Circle",
      "product_quantity": "610 total test kits (PYR and Oxidase)",
      "code_info": "Oxidase kit - lot 2222008 with expiration date 08/31/13",
      "center_classification_date": "20130528",
      "distribution_pattern": "Worldwide Distribution - USA Nationwide and tthe countries of Australia, Canada, Europe, Hong Kong, Mexico, New Zealand, Singapore, and Taiwan.",
      "state": "MD",
      "product_description": "BBL DrySlide Oxidase Kit, catalog number 231746    Product Usage:  Presumptive diagnostic aid for gram-negative bacteria.",
      "report_date": "20130605",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Becton Dickinson & Co.",
      "recall_number": "Z-1423-2013",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "65089",
      "termination_date": "20130928",
      "recall_initiation_date": "20130412",
      "postal_code": "21152-0999",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}