{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Terminated",
      "city": "Triesen",
      "state": "N/A",
      "country": "Liechtenstein",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87094",
      "recalling_firm": "BEMER INT. AG",
      "address_1": "Austrasse 15",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US",
      "recall_number": "Z-1105-2021",
      "product_description": "Bemer-Set/ Pro-Set  for the following models:  REF. 410201 (BEMER Pro-Set), REF. 420201 (B.BOX Professional), REF. 420100 (B.BOX CLASSIC), REF. 410100 (BEMER Classic-Set), REF. 420200 (B.BOX Professional), and REF. 410200  (BEMER Pro - Set)",
      "product_quantity": "197,724 units",
      "reason_for_recall": "There potential that electromagnetic fields generated in the therapy system may cause technical defects in a patient using an insulin pumps or a malfunction of a pacemaker.",
      "recall_initiation_date": "20210113",
      "center_classification_date": "20210210",
      "termination_date": "20230712",
      "report_date": "20210217",
      "code_info": "All Lot Numbers"
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}