{
  "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": "Franklin Lakes",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86679",
      "recalling_firm": "Becton Dickinson & Company",
      "address_1": "1 Becton Dr",
      "address_2": "N/A",
      "postal_code": "07417-1815",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-0508-2021",
      "product_description": "BD Ultra-Fine Pen Needles 32G x 4mm (5/32' )-intended for parenteral administration of a drug from a cartridge contained in a drug pen injector  Catalog Number: 320122",
      "product_quantity": "2,881,200 units",
      "reason_for_recall": "Product shelf cartons incorrectly labeled as products intended for the Latin American market. Although the product description on the label  32G x 4mm pen needles  is correct, information pertinent to users in the US regarding compatibility with specific pen needles is missing.",
      "recall_initiation_date": "20201023",
      "center_classification_date": "20201127",
      "termination_date": "20230908",
      "report_date": "20201209",
      "code_info": "Batch Number: 9352052  Exp. Date: 20241231",
      "more_code_info": ""
    }
  ]
}