{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "30489",
      "product_res_number": "Z-0252-04",
      "event_date_initiated": "2003-11-20",
      "event_date_posted": "2003-12-19",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-02-10",
      "res_event_number": "27764",
      "product_code": "GWD",
      "k_numbers": [
        "K032701"
      ],
      "product_description": "SurgAssist System Circular Stapler DLU 29mm",
      "code_info": "Product Code CS29, Lot numbers LC-000125, LC000126, LC-000127, LC-000131, LC-000132, LC-000133, LC-000137, LC-000139, LC-000139-1, LC-000142, and LC-000143.",
      "firm_fei_number": "3003171713",
      "recalling_firm": "Power Medical Interventions",
      "address_1": "110 Union Square Dr",
      "city": "New Hope",
      "state": "PA",
      "postal_code": "18938-1365",
      "additional_info_contact": "Emmanuel Tribie\n267-775-8100",
      "reason_for_recall": "improper staple formation or anvil jam",
      "root_cause_description": "Other",
      "action": "On 11/20/03, the recalling firm sent recall notices via overnight carrier to all customers who have been shippped and/or sold the product. The recall notice requested the return of the devices.",
      "product_quantity": "1164 units",
      "distribution_pattern": "The products were shipped to medical facilities and sales representatives nationwide. The product was also shipped to distributors in the United Kingdom, France, Scotland, Belgium, Germany, Israel, Italy, Japan, Spain, Portugal, and Sweden.",
      "openfda": {
        "k_number": [
          "K844836",
          "K873299"
        ],
        "device_name": "Indirect Fluorescent Antibody Test, Entamoeba Histolytica & Rel Sp",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.3220",
        "device_class": "2",
        "registration_number": [
          "2031468"
        ],
        "fei_number": [
          "3002023342"
        ]
      }
    }
  ]
}