{
  "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": "2026-10-07",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Alameda",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99591",
      "recalling_firm": "Penumbra Inc.",
      "address_1": "1 Penumbra",
      "address_2": "",
      "postal_code": "94502-7610",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AL, CA, CO, FL, LA, NC, NY, TX, UT, WI.",
      "recall_number": "Z-3331-2026",
      "product_description": "Brand Name: Penumbra System (RED 62 Reperfusion Catheter)  Product Name: Penumbra System (RED 62 Reperfusion Catheter)  Model/Catalog Number: THNDRRED62SKIT  Software Version: N/A  Product Description: Product common name: Percutaneous catheter    A complete product description is provided in Attachment 1 (HHE-2026-002 RED62).  Component: Penumbra System",
      "product_quantity": "43",
      "reason_for_recall": "Due to manufacturing issues reperfusion catheters may fracture.",
      "recall_initiation_date": "20260724",
      "center_classification_date": "20260929",
      "report_date": "20261007",
      "code_info": "Lot Code: UDI: 00815948024359 Lot Number: H00007856",
      "more_code_info": ""
    }
  ]
}