{
  "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": "2026-03-18",
    "results": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Paramus",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90523",
      "recalling_firm": "Touch US Llc",
      "address_1": "94 Lilac Ln",
      "address_2": "",
      "postal_code": "07652-5291",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide Distribution to:   CA,   FL  IL  KY  LA  MA  MD  MI  NC  NH  NJ  NY  OH  OK  OR  PA  TN  TX  VA",
      "recall_number": "Z-1461-2022",
      "product_description": "etouchus, model no. ETM-G01.  Noninvasive Blood glucose meter.",
      "product_quantity": "149",
      "reason_for_recall": "Device was marketed without FDA 510(k) clearance or a PMA.",
      "recall_initiation_date": "20220621",
      "center_classification_date": "20220726",
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      "code_info": "UDI-DI (GTIN): 00195893740581",
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}