{
  "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": "Ongoing",
      "city": "El Segundo",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89880",
      "recalling_firm": "Karl Storz Endoscopy",
      "address_1": "2151 E Grand Ave",
      "address_2": "N/A",
      "postal_code": "90245-5017",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "U.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, Guam, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA,WI, WV, and WY.  O.U.S.: Mexico, Lebanon, and South Korea",
      "recall_number": "Z-1066-2022",
      "product_description": "11274BCU1 11274BCUK1 Flexible Cystoscope Z18449US-BD (08-2018)",
      "product_quantity": "All Serial Numbers manufactured/distributed since January 2018.",
      "reason_for_recall": "Failure to achieve the expected six-log reduction in microorganisms following the disinfection process.",
      "recall_initiation_date": "20220401",
      "center_classification_date": "20220512",
      "report_date": "20220518",
      "code_info": "11274BCU1 11274BCUK1 Flexible Cystoscope Z18449US-BD (08-2018) UDI Code: 4048551408155  All Serial Numbers manufactured/distributed since January 2018."
    }
  ]
}