{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "220279",
      "product_res_number": "Z-2307-2026",
      "event_date_initiated": "2026-04-27",
      "event_date_posted": "2026-06-03",
      "recall_status": "Open, Classified",
      "res_event_number": "98957",
      "product_code": "LRO",
      "product_description": "Aligned Medical AMS16835 Fluids Kit   RX",
      "code_info": "UDI-DI: B098AMS168350;\nLot Numbers: 233828, 236048, 236359, 236662, 238580, 239934, 239935",
      "firm_fei_number": "1000125955",
      "recalling_firm": "Windstone Medical Packaging, Inc.",
      "address_1": "1602 4th Ave N",
      "city": "Billings",
      "state": "MT",
      "postal_code": "59101-1521",
      "reason_for_recall": "Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits.",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "An URGENT: MEDICAL DEVICE RECALL dated 4/27/26 was sent to customers.\n\nPlease Note: Since AMS manufactured convenience kits that contain Huons Co. Ltd. Pharmacy Lidocaine HCL 1% 5ML SDV, we are extending our recall strategy to the end user level.\n\nAMS requests that you undertake the following activities:\n1. Immediately check your inventory for the recalled products listed above and place them under quarantine.\n2. Due to the manufacturing process any finished sterilized packs remaining in inventory, or at your facility will require over labeling for all products affected by this recall. Packs will be labeled with a sticker attached to each pack. This sticker will read:\n\nRECALL NOTICE\nHuons Co. Ltd. announced the recall of 73293-0001-2 Lidocaine Hydrochloride Injection contained in this kit after it was sealed and sterilized. All other components in the kit are not affected by this recall.\n\" At the time the kit is opened for use any Huons Co. Ltd. Lidocaine Hydrochloride Injection should be identified, and quarantined.\n\" The recalled Huons Co. Ltd. Lidocaine Hydrochloride Injection should be rendered unusable to protect against inadvertent use and returned to AMS.\n\n3. Complete the attached Recall Reply Form listing all inventory of affected product by lot number and quantity.\n4. If you have further distributed this product, please identify your distribution partners, and notify them at once of the product recall. Your notification to your customers should include a copy of this notification letter.\n5. Please complete the Recall Reply Form within 5 business days and return via email to fieldcorrectiveaction@alignedmedical.com even if you have no affected product on hand.\n6. Indicate on the Recall Reply Form if a replacement Huons Co. Ltd. product is needed.\n\nIf you have any questions or concerns please do not hesitate to contact us at fieldcorrectiveaction@alignedmedicalsolutions.com.\n\nDear Customer,\nThis letter is to describe the process for placing the \"Recall Notice",
      "product_quantity": "875 kits",
      "distribution_pattern": "US Nationwide distribution in the states of IL, VA.",
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