{
  "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": "2026-07-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Livermore",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99148",
      "recalling_firm": "Penumbra, Inc.",
      "address_1": "6262 Patterson Pass Rd Ste A",
      "address_2": "N/A",
      "postal_code": "94550-9576",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution including in the states and territories of AK, AL, AE, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KY, MA, MD, MI, MN, MO, MS, NC, ND, NE, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, Puerto Rico and the countries of Brazil, Canada, Colombia, Ecuador, Indonesia, Israel, Lebanon, Mexico, Mongolia, Philippines, Saudi Arabia, Thailand, and United Arab Emirates.",
      "recall_number": "Z-2770-2026",
      "product_description": "Penumbra System RED 68 Reperfusion Catheter  REF: RED68KIT",
      "product_quantity": "N/A",
      "reason_for_recall": "Due to manufacturing issues,  reperfusion catheters may fractures",
      "recall_initiation_date": "20260603",
      "center_classification_date": "20260721",
      "report_date": "20260729",
      "code_info": "UDI: 00815948024113/Lots: H00008699, H00008701, H00008702, H00008703, and C00020038"
    }
  ]
}