{
  "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-0567-2015",
      "product_description": "Veta Peritoneal Catheter Kit, Curled, Ref No. M7225    Product Usage:  Veta Peritoneal Dialysis Catheters are intended for acute and chronic access to the peritoneal cavity.",
      "product_quantity": "85 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. 1212-005"
    }
  ]
}