{
  "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": "2026-09-05",
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      "product_res_number": "Z-2763-2026",
      "event_date_initiated": "2026-05-07",
      "event_date_posted": "2026-07-20",
      "recall_status": "Open, Classified",
      "res_event_number": "99249",
      "product_code": "OJK",
      "product_description": "Halyard EYE PACK. Model/Catalog Number: LVEY27\n\nConvenience kit.",
      "code_info": "Model/Catalog Number: LVEY27. UDI-DI: 10809160499528. Lot Numbers (Expiration Date): 1680076 (12/31/2026), 1680590 (6/30/2027).",
      "firm_fei_number": "1047429",
      "recalling_firm": "AVID Medical, Inc.",
      "address_1": "9000 Westmont Dr",
      "city": "Toano",
      "state": "VA",
      "postal_code": "23168-9351",
      "additional_info_contact": "Marlene Jones\n757-566-3510",
      "reason_for_recall": "Incorrect concentration of Betadine solution contained within certain AVID convenience kits.",
      "root_cause_description": "Process control",
      "action": "AVID Medical notified the single consignee on about 05/07/2026 via email. The consignee was instructed to identify, segregate, and quarantine all impacted products, add the provided warning labels to affected AVID kits to ensure all users are aware of the issue, and discard all impacted components upon opening the Eye Pack. Customers and end users were instructed that if they received affected products from a distributor, to please contact that distributor of sales representatives with questions. Distributors were instructed that if any of the affected kits identified were further distributed, to ensure all end-users are appropriately notified and maintain records of effectiveness.  Recipients were requested to complete and return the provided Recall Response Form by 05/22/2026.",
      "product_quantity": "260 kits",
      "distribution_pattern": "US Nationwide distribution in the state of California.",
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