{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Skillman",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65879",
      "recalling_firm": "Convatec Inc.",
      "address_1": "200 Headquarters Park Dr",
      "address_2": "N/A",
      "postal_code": "08558-2600",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-1991-2013",
      "product_description": "ConvaTec Flexi-Seal SIGNAL +,  Rx Only    Product Usage:  For use to manage fecal incontinence through the collection of liquid to semi-liquid stool and to provide access to administer medication.",
      "product_quantity": "22,896 units",
      "reason_for_recall": "ConvaTec notified their customers on 6/25/2013 regarding the manufacturing irregularity that occurred related to the packaging of certain lots of Flexi-Seal Signal FMS.  In certain lots, the lot number convention was duplicated on the packaging.",
      "recall_initiation_date": "20130625",
      "center_classification_date": "20130820",
      "termination_date": "20140108",
      "report_date": "20130828",
      "code_info": "Flexi-Seal Signal + ICC Code 418000; SAP Code# 1705108, Lots 12-FM-01 and 12-FM-02."
    }
  ]
}