{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "67094",
      "product_res_number": "Z-0875-2008",
      "event_date_initiated": "2007-12-03",
      "event_date_posted": "2008-02-13",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-03-31",
      "res_event_number": "46267",
      "product_code": "KPO",
      "k_numbers": [
        "K981003"
      ],
      "product_description": "Dri-Sate Glacial Acidic Acid (liquid component of Dri-Sate Dry Acid Concentrate DR-240); 1 quart (0.95 liters); manufactured by Rockwell Medical Technologies, Inc., Grapevine, TX  76051.",
      "code_info": "Lot #2530-1020052.",
      "firm_fei_number": "3003463852",
      "recalling_firm": "Rockwell Medical Technologies, Inc",
      "address_1": "4051 Freeport Pkwy Ste 100 4051 Freeport Pkwy",
      "address_2": "Ste 100",
      "city": "Grapevine",
      "state": "TX",
      "postal_code": "76099",
      "additional_info_contact": "972-874-2130",
      "reason_for_recall": "Foil Seal Deterioration;  occuring on the tamper resistant foil seals on dialysis liquid concentrate and Dri-Sate product containers older than two years old.",
      "root_cause_description": "Process control",
      "action": "Firm began notification of consignees by letter, Alert: Voluntary Recall, on 12/03/07, sent via e-mail, fax, and/or mail.  Consignees asked to check inventory and to identify and call for the replacement of any product older than 2 years old.",
      "product_quantity": "10 cases (1 one quart bottle per case)",
      "distribution_pattern": "Nationwide Distribution to the following states: AL, AR, FL, KS, LA, MO, MS, OK, TN and TX.",
      "openfda": {
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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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