{
  "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,
      "limit": 1,
      "total": 1
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  },
  "results": [
    {
      "cfres_id": "105069",
      "product_res_number": "Z-0389-2012",
      "event_date_initiated": "2011-09-19",
      "event_date_posted": "2012-01-11",
      "recall_status": "Terminated",
      "event_date_terminated": "2011-12-08",
      "res_event_number": "60344",
      "product_code": "LFQO",
      "product_description": "Magnus Hybrid operating table columns 1180.01A1 and 1180.01B1",
      "code_info": "510 k EXEMPT  1180.01A1- Lot #0002, 0004, 0005, 0007-00011, 00013- 0017, 00019-00029, 00001   1180.01B1- lOT #00001, 00002, 00005-00012, 00014, 00015, 00017, 00018",
      "firm_fei_number": "3008355164",
      "recalling_firm": "Maquet Inc.",
      "address_1": "45 Barbour Pond Drive",
      "city": "Wayne",
      "state": "NJ",
      "postal_code": "07470",
      "additional_info_contact": "Ms. Whitney Torning\n973-709-7660",
      "reason_for_recall": "A component of the Magnus hybrid OR system fails to respond to a position command.",
      "root_cause_description": "Device Design",
      "action": "Maquet sent a PRODUCT RECALL URGENT MEDICAL DEVICE CORRECTIVE ACTION letter dated September 19, 2011, to all affected customers.  The letter identified the product, the problem, and the action to be taken by the customer. To avoid the potential of a malfunction occurring prior to their scheduled Service procedure, customers were instructed to ensure that the MAGNUS table-top is positioned at the \"0\" pivot position and that the MAGNUS column pivot brake is secured.  If it is necessary to pivot the MAGNUS table-top prior to procedure start, ensure that the column pivot brake is completely released and then completely secured when returned to \"0\" pivot position.  Customers were instructed to ensure that all user of the affected product and other necessary persons are informed of the product correction notice.  \nFor technical support or questions call 1-888-627-8383",
      "product_quantity": "45 UNITS",
      "distribution_pattern": "Worldwide Distribution - USA including VA, LA, MO, NC, MD, and AZ and the countries of AE, AU, CA, CH, CN, DE, DK, ES, IE, IL, SP, PL, RU, and TH.",
      "openfda": {}
    }
  ]
}