{
  "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",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "221342",
      "product_res_number": "Z-2858-2026",
      "event_date_initiated": "2026-05-21",
      "event_date_posted": "2026-08-03",
      "recall_status": "Open, Classified",
      "res_event_number": "99338",
      "product_code": "PEV",
      "product_description": "Brand Name: Medical Action Industries \nProduct Name: Dialysis Change Tray Clear Sequence\nModel/Catalog Number: 78791",
      "code_info": "Lot Code: Lot No.: 327075\t328690\t319980\t320965\t318461\t322375\t325653\t330775\t331356\t336680\nUDI: 20809160242558",
      "firm_fei_number": "1030451",
      "recalling_firm": "Medical Action Industries, Inc. 306",
      "address_1": "25 Heywood Rd",
      "city": "Arden",
      "state": "NC",
      "postal_code": "28704-9302",
      "reason_for_recall": "Convenience kits contain  needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "On May 21, 2026 Medical Action Industries issued a \"Urgent: Medical Device\" Recall notification via Email. Medical Action Industries asked consignees to take the following actions:\n\n1. Identify, Segregate, and Quarantine all impacted kits listed in Table 1.\n\n2. Add warning labels to affected AVID kits to ensure all users are aware of discarding the impacted component prior to use. \n3. A labeling template is enclosed for printing labels which can be affixed on all affected kits and cases in inventory. \n\n4. Customers (end-users): If you have received product from a distributor, please contact the distributor or your sales representative with any questions you may have.\n\n5. Distributors: If any of the affected kits identified above were further distributed, please ensure all end-users are appropriately notified and maintain records of effectiveness.\n\n6. Complete the attached Recall Response Form and return by June 5, 2026.",
      "product_quantity": "3740 kits (180 cases)",
      "distribution_pattern": "US Nationwide distribution in the state of CA.",
      "openfda": {
        "device_name": "Dialysis Administration Kit",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.5820",
        "device_class": "2",
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