{
  "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": [
    {
      "country": "United States",
      "city": "Parsippany",
      "address_1": "399 Interpace Pkwy",
      "reason_for_recall": "The products failed the filed specification of 1.0kPa for Burst Pressure.",
      "address_2": "",
      "product_quantity": "487980 condoms",
      "code_info": "Batch Numbers: 1000427177, 1000408620, 1000430764",
      "center_classification_date": "20180924",
      "distribution_pattern": "US Nationwide.",
      "state": "NJ",
      "product_description": "Durex Real Feel Polyisoprene Condoms, 10 count and 24 count, SKU Numbers 02340-89456-14 and 02340-89457-00    Product Usage:  The Durex Synthetic polyisoprene male condom is used for contraception and for prophylactic purposes (to help prevent pregnancy and the transmission of sexually transmitted disease).",
      "report_date": "20181003",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Reckitt Benckiser LLC",
      "recall_number": "Z-3241-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80841",
      "termination_date": "20200305",
      "more_code_info": "",
      "recall_initiation_date": "20180723",
      "postal_code": "07054-1133",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}