{
  "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": "2026-08-20",
    "results": {
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  "results": [
    {
      "cfres_id": "150184",
      "product_res_number": "Z-0390-2017",
      "event_date_initiated": "2016-10-05",
      "event_date_created": "2016-11-10",
      "recall_status": "Terminated",
      "event_date_terminated": "2018-02-02",
      "res_event_number": "75386",
      "product_code": "FQO",
      "product_description": "Accessory Adapter Part number 600525A0\n\nProduct Usage:\ndesigned for the mounting of MAQUET accessories with the dovetail guide interface immediately before, during and after surgical interventions as well as for examination and treatment.",
      "code_info": "600525A0",
      "firm_fei_number": "3008355164",
      "recalling_firm": "Maquet Medical Systems USA",
      "address_1": "45 Barbour Pond Dr",
      "city": "Wayne",
      "state": "NJ",
      "postal_code": "07470-2094",
      "additional_info_contact": "Maquet Customer Service\n888-627-8383",
      "reason_for_recall": "Maquet Inc. is initiating a voluntary field action on the Accessory Adapter part number 600525A0 due to a complaint in which a head rest mounted to the accessory adapter slipped out of the mountain rail.",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "Maquet Medical Systems USA sent an Urgent Product Recall Medical Device Removal letter dated October 5, 2016 to the affected customers.  The letter identified the affected product, problem and actions to be taken.  Customers were instructed to:\n1. Read this Medical Device Removal Notice and disseminate the information\nprovided to all the users of the device.  2. Examine your inventory immediately to determine if you have the Accessory Adapter(s). If so, remove the affected products, quarantine them and keep them in a secure location for shipment back to Maquet. 3. Please fill out and sign the enclosed Medical Device Removal Response Form on page 4 and return it either via  email to FieldActions@maquet.com or fax to 1-973-909-9927.  For question contact your local MAQUET Representative or call MAQUET Customer Service at 1-888-627-8383 (Press option 2, then followed by option 3) Monday through Friday, between the hours of 8:00 a.m. and 5:00 p.m. EDT.",
      "product_quantity": "9 Units (US) 141 Units (OUS)",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of AZ, CA, DC, MI, MO, and PA",
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        "device_name": "Table, Operating-Room, Ac-Powered",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4960",
        "device_class": "1"
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