{
  "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": {
      "skip": 0,
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      "product_res_number": "Z-0102-2022",
      "event_date_initiated": "2020-03-10",
      "event_date_created": "2021-10-13",
      "recall_status": "Terminated",
      "event_date_terminated": "2023-09-22",
      "res_event_number": "88667",
      "product_code": "DRO",
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      "code_info": "All codes",
      "firm_fei_number": "3012307300",
      "recalling_firm": "Smiths Medical ASD Inc.",
      "address_1": "6000 Nathan Ln N",
      "city": "Minneapolis",
      "state": "MN",
      "postal_code": "55442-1690",
      "additional_info_contact": "Dave Halverson\n763-383-3310",
      "reason_for_recall": "Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.",
      "root_cause_description": "Component design/selection",
      "action": "The firm initiated the recall by letter during the week of 03/10/2020.  The notices requested the direct consignee notify their customers and collect the responses.  The firm is seeking return of the products.",
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      "distribution_pattern": "Austria, France, Germany, Great Britain, and Saudi Arabia",
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        "device_name": "Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.5550",
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