{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
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      "cfres_id": "25420",
      "product_res_number": "Z-0478-03",
      "event_date_initiated": "2003-01-08",
      "event_date_posted": "2003-01-30",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-05-01",
      "res_event_number": "25224",
      "product_code": "EMX",
      "k_numbers": [
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      ],
      "product_description": "Ultracell 8.0 cm Nasal Packing w/tube\nCatalog #:10110-CT",
      "code_info": "Lot  Numbers: 063201  Exp. 5/2005                             063202  Exp. 6/2005                             063204  Exp. 7/2005                            063206  Exp. 8/2005                             063208  Exp.  11/2005",
      "firm_fei_number": "1000120594",
      "recalling_firm": "Ultracell Medical Technologies",
      "address_1": "183 Providence",
      "city": "North Stonington",
      "state": "CT",
      "postal_code": "06359",
      "additional_info_contact": "Audrey Vitale\n860-599-4883",
      "reason_for_recall": "Sterility of the device is compromised",
      "root_cause_description": "Other",
      "action": "Ultracell Medical Technologies initiated the recall by fax or mail on 1/8/03. The firm requested return of product . Distributors were requestd to recall to their accounts.",
      "product_quantity": "89.15 boxes",
      "distribution_pattern": "Nationwide",
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