Every recall we track for Getinge Usa Sales Inc — 48 in all — plus the complaints and injury reports the public filed about them.
Getinge recalls specific vaporizers used in anesthesia due to potential hydrogen fluoride release from sevoflurane. This could cause respiratory irritation or severe health issues. Affected models include Flow-i C20, C30, C40.
Getinge recalls MEERA CL mobile operating tables with error code 50037 that may stop movement during use, causing procedural delays. Affected units have specific serial numbers and item numbers.
Getinge recalls MEERA CL mobile operating tables with error code 50037 that may stop movement during use, causing procedural delays. Affected units have specific serial numbers and were sold between 2023 and 2:00 PM on 11/15/2023.
Getinge recalls MEERA CL mobile operating tables that may stop unexpectedly due to error code 50037, causing procedural delays during surgery. Affected units have specific serial numbers and item numbers.
Getinge recalls MEERA CL mobile operating tables with error code 50037 that may cause procedural delays during patient positioning. Affected units have serial numbers 1059-1091. No immediate action needed but check for error code.
Getinge recalls MEERA CL mobile operating tables with error code 50037 that may stop movement during use, causing procedural delays. Affected units have serial numbers 680-707.
Getinge recalls MEERA CL mobile operating tables with error code 50037 that may cause procedural delays during patient positioning. Affected units have specific serial numbers and item numbers.
Getinge recalls ALPHAMAXX mobile operating tables with defective charger units (model 1133.22B4/B5/F5) that may cause inadequate charging and operational failure. Affected units have specific serial numbers and were sold in the U.S. between 2023 and 2024.
Getinge recalls ALPHAMAXX mobile operating tables with defective charger units (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5. This may cause inadequate charging and operational failure.
Getinge recalls ALPHAMAXX mobile operating tables with defective chargers that may cause charging failure. Affected models include 1133.22B4, 1133.22B5, and 1133.22F5 with specific serial numbers. No remedy is stated in the recall notice.
Getinge recalls vaporizers with product code 6682282 (Flow-i C20, C30, C40) due to potential hydrogen fluoride release from sevoflurane. This may cause respiratory irritation, lung edema, or severe hypocalcemia. Affected units have serial numbers 17003-23454.
Getinge recalls Flow-i C40 Anesthesia System model 6677400 due to potential cybersecurity vulnerability that could lead to denial of service, tampering, or remote code execution.
Getinge recalls Flow-i C30 Anesthesia System model 6677300 due to potential cybersecurity vulnerabilities that could allow remote attacks. Affected units include specific serial numbers and UDI-DI codes.
Getinge recalls Flow-e Anesthesia System model 6887900 due to potential cybersecurity vulnerabilities that could lead to denial of service, tampering, or remote code execution.
Getinge recalls Flow-i C20 Anesthesia System model 6677200 due to potential cybersecurity vulnerabilities that could allow remote attacks, leading to system disruption or tampering.
Getinge recalls Flow-c Anesthesia System model 6887700 due to potential cybersecurity vulnerabilities that could allow remote attacks, leading to system failures or tampering during medical use.
Getinge recalls specific Maquet Orchide OR Light Systems models due to potential falling risk in operating rooms. Affected units include OHDII FHD QL VP01 and other variants with unique identifiers. Consumers should check their model numbers and contact Getinge for details.
Getinge recalls specific Maquet Prismalix OR light systems due to potential for falling in operating rooms. Affected models include 3001, 4001, 6001K, and others with catalog numbers starting with ARD567. No remedy is stated in the recall notice.
Getinge recalls specific OR light systems due to potential for falling in operating rooms. Affected models include XTen and X10 series with listed catalog numbers. Consumers should check their product details to determine if recalled.
Getinge recalls certain OR light systems due to potential for falling in operating rooms. Affected models include Hanaulux 2006/2007, Blue 100, Blue 130/90, Blue Series 30/80, and Prismatic OR Light Systems. No model numbers provided.
Getinge recalls Maquet Hanaulux HLX2000 OR Light Systems with specific model numbers due to potential for light systems to fall in operating rooms, posing a risk of injury.
Getinge recalls Maquet Axcel/AXcel+ OR light systems due to potential for light system to fall in operating rooms. Affected models include AXL 5001 series and others. No remedy specified in recall notice.
Getinge recalls specific Maquet G8/G8E OR light systems due to potential falling risk during surgery. Affected models include G8 LC E - ARD568131211C and others. Stop using immediately if you own these models.
Getinge recalls Maquet Hanaulux HLX3000 OR light systems due to potential falling risk during surgery. Affected units have model numbers H3 BC - HM567811111C.
Getinge recalls Volista light systems due to potential for light systems to fall in operating rooms. Affected models include Volista, Volista Access, Volista Access II, and Volista Standop OR Light System with specific model numbers.
Maquet recalls Brainlab camera light systems with specific model numbers due to potential for falling in operating rooms. Affected units include BRAINLAB CAMERA - ARDEQT269000A and other variants.
Getinge
Maquet Lucea light systems with specific model numbers may fall in operating rooms. Affected units include Lucea10/40, Lucea50/100 and various LCA models. Consumers should check their product details.
Getinge recalls specific Maquet Rolite OR light systems due to potential for falling in operating rooms. Affected models include ROL PWDII50SF, ROL PWDII70SF, and others. Stop using immediately to prevent injury.
Getinge recalls Maquet Blueline Series 30/80 OR Light Systems with specific model numbers due to potential for light systems to fall in operating rooms. Affected units include BLUE 30 and BLUE 80 models with catalog numbers starting with ARD569015111A.
Getinge recalls PowerLED/HLED and PowerLED300 OR Light Systems with specific model numbers due to potential for light systems to fall in operating rooms.
Getinge recalls Meera Mobile Operating Tables with model 7200.01F2 that may unintentionally move patients during surgery due to a control unit issue, posing potential injury risks.
Getinge recalls Flow-i C20, C30, and C40 anesthesia systems with software versions 4.8.0-4.8.3 due to a bug that can prevent oxygen delivery, risking hypoxia.
Getinge recalls anesthesia system with software bug that prevents pressure buildup, risking oxygen shortage during surgery. Affected units have specific serial numbers and software versions.
Getinge recalls Flow-e Anesthesia System (part 688: 07325710010457) due to software bug causing ventilation failure. Affected units may not build pressure, risking oxygen shortage.
Getinge recalls Flow-c and Flow-e Anesthesia Systems with specific product codes and serial numbers due to potential backup battery failure during power outages, risking inadequate ventilation support.
Getinge recalls extension tabletops (model 1140.20F0 and 1140.20AN) due to risk of sudden back rest drop causing patient head injury if falling head-first. Product discontinued in 2008.
Getinge recalls ventilators with model 6882000 (serials 10558-24017) due to stability issues. These devices may tip over when stationary, risking injury during use.
Getinge is a leading global manufacturer of medical equipment and surgical instruments. We provide innovative solutions for healthcare professionals worldwide.
Getinge recalls VOLISTA StandOP Surgical Lights with certain product codes due to risk of paint particles detaching during surgery, potentially causing infection or tissue reactions. Affected units include specific model numbers and serial ranges.
Getinge recalls Flow-e Anesthesia Systems with serial numbers 50012-50132 due to potential crack in suction switch that could prevent suction activation during surgery.
Getinge recalls Flow-c Anesthesia Systems with serial numbers 4003-5050 for potential suction switch cracks that could prevent suction activation, risking patient harm during anesthesia procedures.
Getinge recalls CM320-2 Chamber WU Series washer disinfectors due to unverified installation risks. This could cause burns, electric shock, or patient infection. Affected units have specific serial numbers.
Getinge recalls CM320 WUWD series washer-disinfectors due to unverified installation risks. Unaddressed installation could cause burns, electric shock, or injuries. Affected units have specific serial numbers.
Getinge recalls specific washer disinfectors due to inadequate installation documentation risks. Affected models include 9120E, 9125E, 9127E, 9128E, 9122EW, 9128EW. Check serial numbers or UDI codes for recall.
Getinge recalls Sevoflurane vaporizer filling part 6886601 due to potential chemical degradation that may cause hydrogen fluoride inhalation or skin exposure. Affected units include specific anesthesia systems with serial numbers listed in the recall notice.
