{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Parsippany",
      "address_1": "399 Interpace Pkwy",
      "reason_for_recall": "Product marketed in U.S. does not have sufficient data to ensure that it will meet the internal burst pressure specifications at the end of 5 yrs shelf-life",
      "address_2": "",
      "product_quantity": "34 cartons/12 condoms each (408 condoms total)",
      "code_info": "Lot Number - 1000490884",
      "center_classification_date": "20181009",
      "distribution_pattern": "US in the states of NY",
      "state": "NJ",
      "product_description": "Polyisoprene condomns    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": "20181017",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Reckitt Benckiser LLC",
      "recall_number": "Z-0091-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80939",
      "termination_date": "20191112",
      "more_code_info": "",
      "recall_initiation_date": "20180806",
      "postal_code": "07054-1133",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}