{
  "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": "82415",
      "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": "Distributed to accounts in CA  FL  GA  IN  KY  LA  MA  MI  MO  MS  NJ  NY  OH  OK  PA  SC  TN  TX  VA  WV.",
      "recall_number": "Z-1149-2019",
      "product_description": "14F SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061422",
      "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": "20190416",
      "termination_date": "20240305",
      "report_date": "20190424",
      "code_info": "MCAL680  MCBA840  MCBH140  MCBK600  MCBY920  MCCH670  MCCR320  MCCV590  MCDG930  MCDK980  MCDR400  MCFB320  MCFG490  MCFR460  MCFT410  MCFY850  MCFZ660  MKAD410  MKAN270  MKAP300  MKAT100  MKAX320  MKBA190  MKBK940  MKBL210  MKBP450  MKBV570  MMAA170  MMAD480  MMAS020"
    }
  ]
}