{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Orange",
      "address_1": "1717 W Collins Ave",
      "reason_for_recall": "Immersion time stated on the bottle is 45 minutes while the product instructions say 90 minutes.",
      "address_2": "",
      "product_quantity": "31904",
      "code_info": "Part Number: 10-6465 (McKesson Reorder # 341)  Lot Numbers: 16 1250, 16 1274, 16 1324A, 16 1324B, 16 2337, 17 1038, 17 1038A, 17 1083, 17 1193, 17 1262, 17   2122, 17 2142, 17 2219, 17 2306, 17 2347A, 18 1092B, 18 1121, 18 2037, and 18 3164.",
      "center_classification_date": "20190604",
      "distribution_pattern": "AZ, CA, CO, FL, GA, IL, KY, LA, MA, MN, MO, NJ, NY, OH, PA, SC, TN, TX, UT, VA, and WA.",
      "state": "CA",
      "product_description": "Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution",
      "report_date": "20190612",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical",
      "recall_number": "Z-1721-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "82553",
      "termination_date": "20210505",
      "more_code_info": "",
      "recall_initiation_date": "20180713",
      "postal_code": "92867-5422",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}