Home / Brands / Getinge Usa Sales
Getinge Usa Sales Recalls
48 recalls on record · January 19, 2022 to February 19, 2025 · Medical Devices
Recalls by year
22
23
24
25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 19, 2025Medical DevicesFDA
Getinge Usa Sales Inc recalls Vaporizer Sevoflurane, Quik-Fil. Model Number: 6682285. Device is a component of Flow-i C20, Flow-i C30, Flow-i C40, Fl
Hazard: Sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients or health care providers through inhalation and/or skin exposure. Potential harms include irritation of respiratory tract, which in worst case may lead to lung edema and/or severe hypocalcemia, blistering, superficial ulceration, and/or hypomagnesemia.
November 20, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during a
Hazard: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
November 20, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during a
Hazard: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
November 20, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during a
Hazard: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
November 20, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during a
Hazard: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
November 20, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during a
Hazard: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
November 20, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during a
Hazard: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
November 20, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during a
Hazard: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
November 20, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during a
Hazard: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
July 17, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322F5
Hazard: The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5 of the ALPHAMAXX mobile operating table. This issue poses a risk of inadequate charging and operational failure.
July 17, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322B5
Hazard: The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5 of the ALPHAMAXX mobile operating table. This issue poses a risk of inadequate charging and operational failure.
July 17, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322B4
Hazard: The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5 of the ALPHAMAXX mobile operating table. This issue poses a risk of inadequate charging and operational failure.
June 12, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Vaporizer Sevoflurane Maquet Filling, Product code/REF number (6682282), Component of: Flow-i C20, Flow-i C30,Flow-i C40
Hazard: Sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients or health care providers through inhalation and/or skin exposure. Potential harms include irritation of respiratory tract, which in worst case may lead to lung edema and/or severe hypocalcemia, blistering, superficial ulceration, and/or hypomagnesemia.
February 14, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Flow-e Anesthesia System, model 6887900
Hazard: Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous situation.
February 14, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Flow-c Anesthesia System, model 6887700
Hazard: Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous situation.
February 14, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Flow-i C40 Anesthesia System, model 6677400
Hazard: Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous situation.
February 14, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Flow-i C30 Anesthesia System, model 6677300
Hazard: Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous situation.
February 14, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Flow-i C20 Anesthesia System, model 6677200
Hazard: Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous situation.
January 24, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Maquet Hanaulux 2006/ 2007, Blue 100, Blue 130/ 90, Blue Series 30/ 80, and Prismatic OR Light Systems. No Model Number
Hazard: A potential for a light system to fall in the operating room.
January 24, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Maquet Blueline Series 30/80 OR Light Systems, Model Numbers and Catalog Numbers BLUE 30 - ARD569015111A, BLUE 30 - ARD5
Hazard: A potential for a light system to fall in the operating room.
January 24, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Maquet G8 / G8E OR Light Systems, Model Numbers and Catalog Numbers G8 LC E - ARD568131211C, G8G8 DF E - ARD568121111C,
Hazard: A potential for a light system to fall in the operating room.
January 24, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Maquet Hanaulux HLX2000 OR Light Systems, Model Numbers and Catalog Numbers 3001 - ARD567424001C, 3001 HMS07 - ARD567722
Hazard: A potential for a light system to fall in the operating room.
January 24, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Maquet Prismalix OR Light Systems, Model Numbers and Catalog Numbers 3001 - ARD567424001C, 3001 HMS07 - ARD567722001C, 3
Hazard: A potential for a light system to fall in the operating room.
January 24, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Maquet XTen OR Light Systems, Model Numbers and Catalog Numbers 3001 HMD14 - ARD567732001C, X TEN DUO - ARD568221510C, X
Hazard: A potential for a light system to fall in the operating room.
January 24, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Maquet Hanaulux HLX3000 OR Light Systems, Model Numbers and Catalog Numbers H3 BC - HM567811111C
Hazard: A potential for a light system to fall in the operating room.
January 24, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Maquet Axcel / Axcel + OR Light Systems, Model Numbers and Catalog Numbers AXL 5001 - ARD567501961C, AXL 5001S - ARD5675
Hazard: A potential for a light system to fall in the operating room.
January 24, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Maquet PowerLED/HLED and PowerLED300 OR Light Systems, Model Numbers and Catalog Numbers EPS MB1 - ARDINT059002A, EPS MB
Hazard: A potential for a light system to fall in the operating room.
January 24, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Maquet Orchide OR Light Systems, Model Numbers and Catalog Numbers OHDII FHD QL VP01 - ARD568803935, OHDII FHD QL AIR03
Hazard: A potential for a light system to fall in the operating room.
January 24, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Maquet Equipment OR Light Systems, Model Numbers and Catalog Numbers BRAINLAB CAMERA - ARDEQT269000A, BRAINLAB CAMERA -
Hazard: A potential for a light system to fall in the operating room.
January 24, 2024Medical DevicesFDA
Getinge Usa Sales Inc recalls Maquet Rolite OR Light Systems, Model Numbers and Catalog Numbers ROL PWDII50SF - ARDPWT309001A, ROL PWDII50SF - ARDPWT3
Hazard: A potential for a light system to fall in the operating room.