{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Carlsbad",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69666",
      "recalling_firm": "Pfm Medical Inc",
      "address_1": "1815 Aston Ave Ste 106",
      "address_2": "N/A",
      "postal_code": "92008-7340",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of  MA, NC, UT, PA, TX, OH, LA and worldwide to: Germany and Malaysia.",
      "recall_number": "Z-0563-2015",
      "product_description": "Micro Introducer Kit, 5F Micro Introducer Kit, Ref No. M4005    Product Usage: These introducers are used for the percutaneous introduction of therapeutic devices, such as PICCS. The PFM CT PICC catheter is indicated for short or long term peripheral access to the central venous system for intravenous therapy, and power injection of contrast media.",
      "product_quantity": "100 units",
      "reason_for_recall": "PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.",
      "recall_initiation_date": "20141020",
      "center_classification_date": "20141209",
      "termination_date": "20150423",
      "report_date": "20141217",
      "code_info": "Lot No. 1302-014"
    }
  ]
}