{
  "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": "2026-09-12",
    "results": {
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      "cfres_id": "195436",
      "product_res_number": "Z-1688-2022",
      "event_date_initiated": "2022-05-10",
      "event_date_created": "2022-09-08",
      "recall_status": "Open, Classified",
      "res_event_number": "90693",
      "product_code": "OXQ",
      "product_description": "VYGON DRESSING CHANGE W/MAXISWAB kit, REF AMS-8465CS",
      "code_info": "Part Number AMS-8465CS, UDI/DI: 00849884005622, Lot Number: 220614962, Expiration Date: 04/30/2023",
      "firm_fei_number": "1450943",
      "recalling_firm": "Stradis Healthcare",
      "address_1": "3600 Burwood Dr",
      "city": "Waukegan",
      "state": "IL",
      "postal_code": "60085-8399",
      "additional_info_contact": "Phil Tobin\n847-596-7740",
      "reason_for_recall": "Potential for incomplete seals.",
      "root_cause_description": "Other",
      "action": "Stradis notified its sole consignee initially by telephone on 05/10/2022 and followed with a letter disseminated by email on 05/11/2022.  The letter explained the problem, risk to health, and requested the quarantine of the affected product pending return.  The letter directed the consignee to notify their customers to whom they further distributed the product to return the product to Stradis.",
      "product_quantity": "520 units",
      "distribution_pattern": "Pennsylvania",
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