{
  "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": "Terminated",
      "city": "Scottsdale",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87432",
      "recalling_firm": "Sharp Medical Products",
      "address_1": "14362 N Frank Lloyd Wright Blvd",
      "address_2": "N/A",
      "postal_code": "85260-8846",
      "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.:  AZ, FL, MI, OH, TX, and WI.    O.U.S.: None",
      "recall_number": "Z-1366-2021",
      "product_description": "SHARP MEDICAL PRODUCTS, LLC Reactor and Sleeve REF 100-36-01 Size: Adult",
      "product_quantity": "129 units (63 units for Human-use and 66 units for Non-Human use)",
      "reason_for_recall": "Non-conformity (holes/punctures or deep creases) in the sterile barrier.",
      "recall_initiation_date": "20210208",
      "center_classification_date": "20210406",
      "termination_date": "20230217",
      "report_date": "20210414",
      "code_info": "Catalogue Number: 100-36-01  Lot Number:  0818-009"
    }
  ]
}