{
  "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-2215-2019",
      "product_description": "14F x 20CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061423     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": "MCAK580 MCAS990 MCAY850 MCBA850 MCBH150 MCBN670 MCBY930 MCCC770 MCCK640 MCCN740 MCCR330 MCCW790 MCDC600 MCDK990 MCDR410 MCFB340 MCFG840 MCFL120 MCFP220 MCFT420 MCFZ280 MKAF340 MKAG480 MKAN280 MKAT110 MKAX330 MKBA730 MKBH920 MKBN710 MKBX790 MMAB370 MMAD450 MMAQ940"
    }
  ]
}