{
  "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": "Peachtree Corners",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89046",
      "recalling_firm": "Stradis Medical, LLC dba Stradis Healthcare",
      "address_1": "3025 Northwoods Pkwy",
      "address_2": "N/A",
      "postal_code": "30071-1524",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "NJ, MI, MA, NY, TX, CO, NC, CT, OR, OH",
      "recall_number": "Z-0400-2022",
      "product_description": "Custom Assemblies, Inc., Single Spike Tumescent Set w/o Chamber, Reorder Number CMS-1212NS Bulk",
      "product_quantity": "620 tube sets",
      "reason_for_recall": "This recall has been initiated to address bulk packed, non-sterile Intravascular Administration Sets that were erroneously distributed to fill orders for the sterile version of the same Intravascular Administration Set.",
      "recall_initiation_date": "20211028",
      "center_classification_date": "20211220",
      "termination_date": "20230807",
      "report_date": "20211229",
      "code_info": "Lot code 20519-2103"
    }
  ]
}