Home / Brands / Getinge Group Logistics America
Getinge Group Logistics America Recalls
4 recalls on record · October 21, 2020 to March 31, 2021 · Medical Devices
Recalls by year
20
21
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
March 31, 2021Medical DevicesFDA
Getinge Group Logistics America, LLC recalls Operating Table System
Hazard: There is a potential for hydraulic leakage at the inclination function to occur resulting in an unintended Trendelenburg or anti-Trendelenburg movement of the table top depending on patient positioning which may lead to the patient having to be transferred to another OR table causing a delay in the procedure.
March 17, 2021Medical DevicesFDA
Getinge Group Logistics America, LLC recalls Anesthesia gas-machine - Product Usage: intended for use in administering anesthesia while controlling the entire ventil
Hazard: Maquet Critical Care AB received complaints where the FiCO2 value was not zero or as close to zero as expected and/or experienced System Check Out failures when docking the absorber to the Flow i Anesthesia machine.
February 24, 2021Medical DevicesFDA
Getinge Group Logistics America, LLC recalls Getinge CM320 Series Washer Disinfector - Product Usage: A multi chamber washer disinfector intended for washing, disinf
Hazard: The potential that the plastic inlet hose connections may deform or break as a result of material fatigue and/or over tightening of the clamps. A broken hose connection may lead to a hazardous situation of water leakage or water spray. The water leakage or water spray may result in a burn to the user and/or an inconvenience due to a procedural delay if the Washer Disinfector is taken out of service.
October 21, 2020Medical DevicesFDA
Getinge Group Logistics America, LLC recalls Servo-i Ventilator, Part No. 6487800, UDI Code 07325710000823 - Product Usage: intended for general and critical ventila
Hazard: A potentially shorter than specified nebulizer connector may result in difficulty in installing the Aeroneb Nebulizer module to the Servo-i device successfully.