{
  "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": {
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  "results": [
    {
      "cfres_id": "73774",
      "product_res_number": "Z-0161-2009",
      "event_date_initiated": "2008-09-26",
      "event_date_posted": "2008-10-16",
      "recall_status": "Terminated",
      "event_date_terminated": "2009-04-16",
      "res_event_number": "49545",
      "product_code": "FQO",
      "product_description": "Accessory Head Rest for Alphastar Operating Tables",
      "code_info": "USA Part Number 1130.67F0, No serial numbers",
      "firm_fei_number": "3008355164",
      "recalling_firm": "MAQUET Inc.",
      "address_1": "1140 Us Highway 22 Ste 202 1140 Us Highway 22",
      "address_2": "Ste 202",
      "city": "Bridgewater",
      "state": "NJ",
      "postal_code": "08807-2958",
      "additional_info_contact": "Mr. Jamie Yieh\n732-667-1896",
      "reason_for_recall": "During installation or cleaning there is a risk of crushing the finger by handling the head rest in the area of the gas strut while simultaneously actuating the release lever.",
      "root_cause_description": "Other",
      "action": "Urgent Device Correction letters were sent beginning September 26, 2008 via Fed Ex.  Letters identified the potential for finger crush in conjunction with the head rest.  Proper operating instructions are provided as well as a warning sticker to be applied to the head rest indicating proper  positioning.   All letters included a customer response form to be completed by each institution.  Information requested is: that device correction letter has been read and instructions followed; that the corrected operating instructions have been received; that the warning sticker has been properly placed on the headrest, or that they do not have the head rest identified in the device correction letter.  Questions should be addressed to USA Maquet Inc at 1-888-627-8383 #1.",
      "product_quantity": "88 units in US; 1884 units worldwide",
      "distribution_pattern": "Nationwide Distribution",
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        "device_name": "Table, Operating-Room, Ac-Powered",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4960",
        "device_class": "1"
      }
    }
  ]
}