Safety Alert for Trade name: SURGICAL TABLES. Technical name: SURGICAL TABLES. ANVISA registration number: 80259110065. Risk class: - Low Risk. Model affected: MOBILE SURGICAL TABLES. Serial numbers affected: All units manufactured in the period between 2009 and 2013.

According to Agência Nacional de Vigilância Sanitária (ANVISA), this safety alert involved a device in Brazil that was produced by MAQUET DO BRASIL EQUIPAMENTOS MEDICOS LTDA.; MAQUET GmbH.

What is this?

Alerts provide important information and recommendations about products. Even though an alert has been issued, it does not necessarily mean a product is considered to be unsafe. Safety Alerts, addressed to health workers and users, may include recalls. They can be written by manufacturers, but also by health officials.

Learn more about the data here
  • Type of Event
    Safety alert
  • Event ID
    2053
  • Date
    2016-10-17
  • Event Country
  • Event Source
    ANVISA
  • Event Source URL
  • Notes / Alerts
    Brazilian data is current through June 2018. All of the data comes from Anvisa, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Brazil.
  • Extra notes in the data
    According to the company, since they can not ensure that other Devices affected by improperly welding have been placed on the market, the component of all possibly affected Devices (1002.65A0) manufactured within the period between 2009 and 2013 will be replaced . In this way, MAQUET's service department or a service technician authorized by MAQUET will contact the customer to arrange a replacement date without charge. The device must be inspected before any use until replacement is performed. In this particular context, special attention should be paid to possible cracks in the weld. According to the company, so far, no incident has been reported in which someone has been injured. It is likely that the break was caused due to improperly welded together with rough handling and multiple application of overload by the user, respectively. ATTENTION: If in doubt, it is advisable that the Device is not used. ### UPDATED ON 10/16/2017, company forwarded evidence and documents proving the correction of the parts and closing the field action. If you wish to notify technical complaints and adverse events use the following channels: Notivisa: Notices of adverse events (AE) and technical complaints (QT) for products subject to Sanitary Surveillance should be made through the NOTIVISA System. To access the System, you must register and select the Health Professional option, if you are a liberal professional or the Institution / Entity option, if you are a professional of an institution / entity. Technovigilance System: Patient or citizen can notify through the Technovigilance System / SISTEC access through the link
  • Reason
    Maquet gmbh cases were reported to have shown that the joint welded between the square structure and the first fixable swivel axis has been broken. this joint must withstand the highest loads due to the cantilever. it is likely that the break was caused due to improperly welded together with rough handling and multiple application of overload by the user, respectively. if the weld is broken during a procedure, there is no avoiding a mechanical injury.
  • Action
    Field Action Code CAPA 2016-008 triggered under the responsibility of the company MAQUET DO BRASIL EQUIPAMENTOS MEDICOS LTDA. Company will make field correction to replace the compromised component.

Manufacturer

  • Manufacturer Parent Company (2017)
  • Source
    ANVSANVISA