{
  "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": "Parsippany",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81964",
      "recalling_firm": "Reckitt Benckiser LLC",
      "address_1": "399 Interpace Pkwy",
      "address_2": "N/A",
      "postal_code": "07054-1133",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide domestic distribution. Foreign distribution to Barbados, Jamaica, Aruba, Guyana, Haiti, and St Maarten.",
      "recall_number": "Z-0994-2019",
      "product_description": "Durex Pleasure Pack (60 ct), synthetic polisoprene male condom, SKU 02340-98729-00  02340-98729-00  02340-98729-00  02340-98729-00  02340-98729-00  02340-98729-00",
      "product_quantity": "34920",
      "reason_for_recall": "Five batches of the product have failed the specification of 1.0kPa for Burst Pressure.",
      "recall_initiation_date": "20181219",
      "center_classification_date": "20190308",
      "termination_date": "20210326",
      "report_date": "20190320",
      "code_info": "WO00905865  WO00905864  WO00901945  WO00900899  WO00900900  WO00900901"
    }
  ]
}