{
  "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-2407-2026",
      "event_date_initiated": "2026-04-30",
      "event_date_posted": "2026-06-11",
      "recall_status": "Open, Classified",
      "res_event_number": "99021",
      "product_code": "OJH",
      "product_description": "Halyard, Pain Pack. Kit Code: AMPK48-01.",
      "code_info": "Kit Code: AMPK48-01. UDI-DI: 10809160472798. Lot Number: 334669. Expiration Date: 8/27/2028.",
      "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": "Inadvertent distribution of sealed pouches that had not undergone validated sterilization.",
      "root_cause_description": "Process control",
      "action": "AVID Medical notified consignees on about 04/30/2026 via emailed letter. Consignees were instructed to identify, segregate and quarantine all affected units on hand, discard all impacted kits and complete and return the provided Response Form. Distributors were instructed to ensure all end-users are appropriately notified and maintain records of effectiveness.",
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      "distribution_pattern": "US Nationwide distribution in  the state of Iowa.",
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