{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
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  "results": [
    {
      "cfres_id": "30620",
      "product_res_number": "Z-0234-04",
      "event_date_initiated": "2003-12-02",
      "event_date_posted": "2003-12-17",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-05-15",
      "res_event_number": "27842",
      "product_code": "MPB",
      "k_numbers": [
        "K030209"
      ],
      "product_description": "Mahurkar QPlus Dual Lumen Catheter Insertion Tray with Curved Extension,   13.5 Fr/Ch x 19.5cm \nFor hemodialysis, apheresis, and infusion\nReference: 8888-135195",
      "code_info": "Lot Number: 140774",
      "firm_fei_number": "1282497",
      "recalling_firm": "Kendall Healthcare Products Co",
      "address_1": "15 Hampshire St",
      "city": "Mansfield",
      "state": "MA",
      "postal_code": "02048-1113",
      "additional_info_contact": "David Olson\n508-261-8530",
      "reason_for_recall": "Product is mislabeled  to catheter length. Product labeled as a 13.5 Fr x 19.5 cm may contain a \n13.5 Fr x 16.0 cm",
      "root_cause_description": "Other",
      "action": "Kendall''s recall letters requesting product return will be hand delivered to customers by Kendall sales representatives on December 1, 2003.",
      "product_quantity": "10",
      "distribution_pattern": "IL, MA,  OH, TN, TX, VA",
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        "device_name": "Catheter, Hemodialysis, Non-Implanted",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.5540",
        "device_class": "2"
      }
    }
  ]
}