{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "93863",
      "product_res_number": "Z-0019-2011",
      "event_date_initiated": "2010-08-10",
      "event_date_posted": "2010-10-07",
      "recall_status": "Terminated",
      "event_date_terminated": "2016-04-22",
      "res_event_number": "56536",
      "product_code": "GBS",
      "product_description": "HydraGlide Silicone Chest Tube Catheter, 24 Fr Straight\nProduct Code 14124",
      "code_info": "Lot 10633072",
      "firm_fei_number": "3011175548",
      "recalling_firm": "Atrium Medical Corporation",
      "address_1": "5 Wentworth Dr",
      "city": "Hudson",
      "state": "NH",
      "postal_code": "03051",
      "additional_info_contact": "Joseph DePaolo\n603-880-1433",
      "reason_for_recall": "Mislabeled: One lot of 24Fr Straight Catheters packaged and labeled as 32Fr Straight Catheters.",
      "root_cause_description": "Packaging process control",
      "action": "Atrium Medical isued Product Recall Notice letters dated August 10, 2010 to customers, identifying the affected product and actions to be taken by customers. Customers were instructed to remove the affected products from inventory and return them to Atrium, and complete and fax a recall notice acknowledgement to Atriuim at 603-821-1420. \nCustomers can contact Atrium at 800 528-7486, x5350 (Joe DePaolo) or x5351 (Karen Hall) for further information.",
      "product_quantity": "10 cases, 10/case",
      "distribution_pattern": "Nationwide Distribution: USA, including the states of AK, CT, OH, and UT.",
      "openfda": {
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          "K851048",
          "K852241",
          "K810158",
          "K912645",
          "K863247",
          "K881873",
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        "device_name": "Catheter, Ventricular, General & Plastic Surgery",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4200",
        "device_class": "1"
      }
    }
  ]
}