{
  "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": "2026-08-13",
    "results": {
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      "product_res_number": "Z-0226-2026",
      "event_date_initiated": "2025-07-25",
      "event_date_posted": "2025-10-21",
      "recall_status": "Open, Classified",
      "res_event_number": "97350",
      "product_code": "QRL",
      "k_numbers": [
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      "code_info": "UDI-DI code / Size:\n06949517008861  / 30g\nLot Number: 2312290802\n\n06949517008854 / 28g\nLot Number: 2406310201\n\n06949517008847 / 23g\nLot Number: 2406310201",
      "firm_fei_number": "3021186226",
      "recalling_firm": "Home Health US, Incorporated",
      "address_1": "7672 15th St E",
      "city": "Sarasota",
      "state": "FL",
      "postal_code": "34243-3213",
      "additional_info_contact": "Luca Hanson\n941-302-0572",
      "reason_for_recall": "Due to incorrect/lack of Unique Device Identifier (UDI) codes.",
      "root_cause_description": "Error in labeling",
      "action": "On 07/25/2025, the firm indicated that they notified Amazon of the recall (mis-labeling) and Amazon has returned affected products that Amazon had in their possession.",
      "product_quantity": "4,661 lancets",
      "distribution_pattern": "U.S.: Nation-wide distributed thru Amazon  U.S. States include: AZ, CA, FL, IL, NC, NM, NY, TN, TX,  and VA.\n\nO.U.S.: N/A",
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        "device_name": "Multiple Use Blood Lancet For Single Patient Use Only",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4850",
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}