{
  "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": [
    {
      "status": "Terminated",
      "city": "Harleysville",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83324",
      "recalling_firm": "Medical Components, Inc dba MedComp",
      "address_1": "1499 Delp Dr",
      "address_2": "N/A",
      "postal_code": "19438-2936",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution CA FL GA IN KY LA MA MI MO MS NJ NY OH OK PA SC TN TX VA WV.",
      "recall_number": "Z-2217-2019",
      "product_description": "14F x 30CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061425     Product  Usage: An aid for introducing a hemodialysis catheter",
      "product_quantity": "6830",
      "reason_for_recall": "Tray label indicates the kits are packaged with a 15F \"valved\" peelable introducer, but the kits contain a 15F \"non-valved\" peelable introducer.",
      "recall_initiation_date": "20190313",
      "center_classification_date": "20190807",
      "termination_date": "20240305",
      "report_date": "20190814",
      "code_info": "MCAM240 MCBL480 MCBS870 MCCF480 MCCJ320 MCCW690 MCCZ500 MCFG830 MCFR160 MCFS760 MCFZ360 MKAJ330 MKAR130 MKBL500 MKBX060 MMAB730"
    }
  ]
}