{
  "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",
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      "res_event_number": "25224",
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      "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.",
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        "device_name": "Sponge, Ophthalmic",
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