{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "South Jordan",
      "address_1": "1600 W Merit Pkwy",
      "reason_for_recall": "Mix-up between adult and pediatrics PD catheter.",
      "address_2": "",
      "product_quantity": "",
      "code_info": "Catalog Number: CF-5242  Lot Numbers: H1027245, H1038032, H1040946, H1063581, H1082840, H1117442, H845164, H879797, H936407, H980897, and H995076.",
      "center_classification_date": "20180814",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of AL, CA, DE, FL, KY, MA, MO, NC, NY, OH, PA, and UT and the countries of Germany",
      "state": "UT",
      "product_description": "Flex-Neck Classic Peritoneal Dialysis Catheter (Pediatric)    Product Usage:  If the patient is a suitable candidate for peritoneal dialysis (PD) therapy, The Flex-Neck¿ PD Catheter can be implanted either surgically or peritoneoscopically. The only contraindication to implantation of the FlexNeck PD Catheter is if the patient is not a candidate for peritoneal dialysis. Numerous prior surgeries or suspected or documented intraperitoneal adhesions may be relative contraindications to PD. However, since the Y-TEC¿ System of peritoneoscopic implantation enable inspection of the peritoneum to confirm the presence of adhesions and to avoid them, all patients who are suitable for PD can receive this catheter.",
      "report_date": "20180822",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Merit Medical Systems, Inc.",
      "recall_number": "Z-2823-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80651",
      "termination_date": "20201029",
      "more_code_info": "",
      "recall_initiation_date": "20171220",
      "postal_code": "84095-2416",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}