{
  "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": "2026-09-10",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 6
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  "results": [
    {
      "cfres_id": "217474",
      "product_res_number": "Z-0987-2026",
      "event_date_initiated": "2025-11-05",
      "event_date_posted": "2025-12-23",
      "recall_status": "Open, Classified",
      "res_event_number": "97989",
      "product_code": "KPO",
      "k_numbers": [
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      "product_description": "Brand Name: Diasol\nProduct Name:  100225-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 liters",
      "code_info": "UDI: None; Lot Code: \n\nPHV07181\tPHV07211\tPHV07231\tPHV07251\tPHV07281\tPHV07282\tPHV07301\tPHV07302\tPHV07311\tPHV08011\tPHV08041\tPHV08051\tPHV08061\tPHV08071\tPHV08111\tPHV08121\tPHV08131\tPHV08132\tPHV08141\tPHV08151\tPHV08181\tPHV08251\tPHV08252\tPHV09021\tPHV09041\tPHV09081\tPHV09091\tPHV09121\tPHV09151\tPHV09161\tPHV09181\tPHV09191\tPHV09221\tPHV09231\tPHV09291\tPHV10031\tPHV10061\tPHV10081\tPHV10091\tPHV10131",
      "firm_fei_number": "3007137482",
      "recalling_firm": "Diasol, Inc",
      "address_1": "310 S 43rd Ave Ste B 310 S 43rd Ave",
      "address_2": "Ste B",
      "city": "Phoenix",
      "state": "AZ",
      "postal_code": "85009-4606",
      "additional_info_contact": "Monica Abeles\n1-602-4427670",
      "reason_for_recall": "Safety and efficacy of dialysis acid concentrate cannot be assured",
      "root_cause_description": "Process design",
      "action": "On November 5, 2025, Diasol issued a \"Urgent Medical Device Recall Notification to affected consignees. In addition to informing consignees about the recall, Diasol asked consignees to take the following actions:\n\n1. Please return all product you have at your facility. \n2. Please complete the attached acknowledgement form. \n3. If product has been further distributed to other distributors, customer or sites, notify those consignees and provide them with a copy of the recall notification.\n4. The notice should be provided to all staff members who use the product. \n5. In the event you have not received adequate products from Rockwell you may continue to use Diasol Products at risk.",
      "product_quantity": "186,000 containers",
      "distribution_pattern": "US Nationwide distribution in the states of MO, CA, AZ, TX, IL, MA.",
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        "device_name": "Dialysate Concentrate For Hemodialysis (Liquid Or Powder)",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.5820",
        "device_class": "2",
        "registration_number": [
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