Events

Recall of Device Recall RotoRest Delta Advanced Therapy System

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Arjo Hospital Equipment AB.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    69970
  • Event Risk Class
    Class 2
  • Event Number
    Z-1216-2015
  • Event Initiated Date
    2014-12-03
  • Event Date Posted
    2015-02-27
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2015-10-30
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=132053
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    Bed, patient rotation, powered - Product Code IKZ
  • Reason
    The recalled devices labeling and instructions for use contain unapproved medical claims.
  • Action
    Devices in the rental fleet will be delivered to the customer with revised documents including the updated information. The customers who purchased the devices will be notified of the recall via letter sent by registered mail. The field correction notice will include a recall letter, response form, and updated labeling.

Device

Device Recall RotoRest Delta Advanced Therapy System
  • Model / Serial
    SERIAL NUMBERS:  RRHK00122,  00157053, RRHK00063, RRHK00123, 00157182, 00157217, 00157058, RRHK00060, 00157184, 00157346, RRHK00110, RRHK00119, 00157373, 00157027, 00157074, 00157220, 00157423, 00157088, 00157302, 00157365, RRHK00112, RRHK00001, RRHK00116, RRHK00003, 00157200, RRHK00014, 157030, 00157461, 00157464, 00157089, 00157304, 00157299, RRHK00121, 00157264, RRHK00071, RRHK00007, 00157243, 00157086, 00157432, RRHK00067, RRHK00097, 00157159, 00157258, 00157362, RRHK00118, RRHK00099, 00157230, RRHK00036, 00157471, 00157013, RRHK00015, 00157203, RRHK00005, 00157014, 00157358, 00157007, 00157344, 00157161, 00157426, RRHK00037, 00157295, 00157054, 00157308, 00157189, RRHK00069, 00157126, RRHK00098, 00157097, RRHK00006, RRHK00120, RRHK00102, RRHK00004, RRHK00101, 00157348, RRHK00107, 00157196, RRHK00066, RRHK00044, 00157303, RRHK00002, 00157305, 00157240, 00157194, 00157244, RRHK00016, 00157321, RRHK00093, 00157067, 00157123, 00157467, 00157465, 00157063, 00157398, 00157387, 00157388, 00157298, 00157313, 00157389, 00157233, 00157101, 00157363, 00157458, RRHK00068, RRHK00113, RRHK00040, 00157330, 00157404, 00157428, RRHK00009, 00157072, RRHK00034, RRHK00041, RRHK00086, RRHK00089, 00157412, 00157430, RRHK00026, 00157062, 00157134, 001P57000, 00157042, RRHK00072, 00157379, RRHK00088, 00157124, 00157232, 00157399, 00157413, RRHK00017, 00157107, 00157160, RRHK00038, 00157376, RRHK00035, RRHK00090, 00157076, 00157251, 00157384, 00157383, 00157129, 00157393, RRHK00031, RRHK00032, 00157094, 00157125, 00157152, 00157130, 00157287, 00157366, RRHK00020, 00157319, 00157445, 00157394, 00157474, RRHK00115, 00157249, 00157453, 00157163, 00157236, RRHK00022, RRHK00025, 00157108, 00157078, 00157135, RRHK00023, 00157335, 00157337, RRHK00024, 00157390, 00157357, RRHK00073, RRHK00018, RRHK00114, RRHK00076, RRHK00092, RRHK00033, RRHK00039, RRHK00027, RRHK00043, RRHK00094, RRHK00095, 00157425, RRHK00028, 00157452, 00157468, RRHK00011, RRHK00070, 00157043, 00157361, RRHK00091, 00157429, RRHK00056, RRHK00057, RRHK00062, 00157037, 00157102, 00157151, 00157153, RRHK00008, RRHK00104, RRHK00105, RRHK00124, 00157104, RRHK00046, RRHK00049, RRHK00051, 00157147, 00157224, RRHK00079, RRHK00083, RRHK00084, RRHK00082, 00157178, 00157214, 00157186, RRHK00080, RRHK00054, 00157262, 00157409, 00157222, 00157381, 00157434, RRHK00047, 00157442, RRHK00050, 00157378, 00157488, RRHK00048, RRHK00058, 00157447, RRHK00085, 00157132, 00157339, RRHK00064, RRHK00055, 00157171, 00157026, RRHK00108, RRHK00021, RRHK00019, 00157080, RRHK00029, RRHK00111, 00157261, 00157407, 00157414, 00157145, 00157149, 00157315, 00157355, 00157202, RRHK00042, 00157451, 00157172, 00157386, 00157060, 00157448, RRHK00077, 00157209, RRHK00061
  • Product Classification
    Physical Medicine Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution. US nationwide, Germany, Austria, France, Italy, India, EU, Mexico, Switzerland, Canada, Saudi Arabia, Kuwait, Middle East, China, Japan, and Qatar.
  • Product Description
    RotoRest Delta Advanced Therapy System. || The RotoRest Delta Advanced Kinetic Therapy System offers kinetic therapy for the most aggressive treatment of pulmonary complications.
  • Manufacturer
    Arjo Hospital Equipment AB

Manufacturer

Arjo Hospital Equipment AB
  • Manufacturer Address
    Arjo Hospital Equipment AB, HANS MICHELSENSGATAN 10, Malm¿ Sweden
  • Manufacturer Parent Company (2017)
    Getinge AB
  • Source
    USFDA