{
  "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-0993-2019",
      "product_description": "Durex Real Feel, synthetic polisoprene male condom, SKU 02340-89456-14  02340-89455-00  02340-89456-14  02340-89456-14  02340-89455-00  02340-95767-00  02340-89456-14  02340-89457-00  02340-89456-14  02340-89456-14  02340-89455-00  02340-89455-00  02340-95767-00  02340-95767-00",
      "product_quantity": "1761044",
      "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": "1000314778  1000289702  1000322841  1000329839  1000317735  1000323210  1000318792  1000170515  1000240186  1000378288  1000183941  1000350794  1000270527  1000277098"
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}