{
  "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": "2026-09-20",
    "results": {
      "skip": 0,
      "limit": 1,
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      "product_res_number": "Z-2517-2025",
      "event_date_initiated": "2025-08-07",
      "event_date_posted": "2025-09-04",
      "recall_status": "Open, Classified",
      "res_event_number": "97427",
      "product_code": "DPW",
      "k_numbers": [
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      "product_description": "FloPatch FP120, REF: FP120-FOT01-005",
      "code_info": "UDI-DI: 10627987360148. Lot: 03250602",
      "firm_fei_number": "3015139886",
      "recalling_firm": "Flosonics Medical (R/A 1929803 ONTARIO CORP.)",
      "address_1": "Fourth Floor, Oneeleven 325 oneeleven front st w",
      "address_2": "Fourth Floor",
      "city": "Toronto",
      "country": "Canada",
      "reason_for_recall": "Flowmeter patch as a human readable expiry date on the outer shipping packaging that reads 2025-06-20 when it should read 2026-06-20.",
      "root_cause_description": "Labeling Change Control",
      "action": "On 8/7/2025, recall notices were emailed to customers who were asked to do the following:\n1. Customers to confirm receipt of recall notice. \n2. Customers should dispose of the outer shipping packaging. \n3. If desired, customers may request replacement product.\n\nFor questions, please contact: cchin@flosonicsmedical.com",
      "product_quantity": "9",
      "distribution_pattern": "US Nationwide distribution in the state of California.",
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