Getinge Usa Sales Inc recalls
Every recall we track for Getinge Usa Sales Inc — 48 in all, from 2021–2025 — plus the complaints and injury reports the public filed about them. 4 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Getinge Usa Sales Inc fell by more than half in 2025 (1, down from 12 in 2024). 8% rated “stop using now”.
All FDA recall records for Getinge Usa Sales Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 1 | 0 | 0 | 0 | 1 |
| 2022 | 0 | 11 | 1 | 1 | 13 |
| 2023 | 2 | 13 | 1 | 5 | 21 |
| 2024 | 1 | 2 | 9 | 0 | 12 |
| 2025 | 0 | 1 | 0 | 0 | 1 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Getinge Usa Sales Inc recalls
What to do if you have a recalled Getinge Usa Sales Inc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Getinge Usa Sales Inc recalls
17 shown- Use cautionMedical device
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,
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.
GetingeJan 15, 2025 - Use cautionMedical device
Getinge Usa Sales Inc recalls MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during
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.
GetingeOct 3, 2024 - Lower riskMedical device
Getinge Usa Sales Inc recalls ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322B4
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.
GetingeMay 29, 2024 - Stop using nowMedical device
Getinge Usa Sales Inc recalls Vaporizer Sevoflurane Maquet Filling, Product code/REF number (6682282), Component of: Flow-i C20, Flow-i C30,Flow-i
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.
GetingeMay 1, 2024 - UnratedMedical device
Getinge Usa Sales Inc recalls Flow-c Anesthesia System, model 6887700
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.
GetingeDec 11, 2023 - Use cautionMedical device
Getinge Usa Sales Inc recalls Maquet PowerLED/HLED and PowerLED300 OR Light Systems, Model Numbers and Catalog Numbers EPS MB1 - ARDINT059002A, EPS
Getinge recalls PowerLED/HLED and PowerLED300 OR Light Systems with specific model numbers due to potential for light systems to fall in operating rooms.
GetingeNov 8, 2023 - Use cautionMedical device
Getinge Usa Sales Inc recalls Meera Mobile Operating Table-to support and position the patient immediately before, during and after surgical
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.
GetingeSep 6, 2023 - Use cautionMedical device
Getinge Usa Sales Inc recalls Getinge Flow-e Anesthesia System, Part No. 6887900
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.
GetingeDec 22, 2022 - Use cautionMedical device
Getinge Usa Sales Inc recalls Flow-c Anesthesia System (Product Code 6887700) Flow-e Anesthesia System (Product Code 6887900)
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.
GetingeNov 7, 2022 - Use cautionMedical device
Getinge Usa Sales Inc recalls Extension Tabletop for Operating Table System 1140, Model Nos. 1140.20F0 and 1140.20AN
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.
GetingeOct 14, 2022 - Use cautionMedical device
Getinge Usa Sales Inc recalls Servo-air Ventilator System-The Servo-air Ventilator System is: Intended for respiratory support, monitoring and
Getinge recalls ventilators with model 6882000 (serials 10558-24017) due to stability issues. These devices may tip over when stationary, risking injury during use.
GetingeJul 21, 2022 - Lower riskMedical device
Getinge Usa Sales Inc recalls Maquet Critical Care AB/Getinge Servo-u Ventilator System, Part Number 6694800 Servo-n Ventilator System, Part Number
Getinge is a leading global manufacturer of medical equipment and surgical instruments. We provide innovative solutions for healthcare professionals worldwide.
GetingeJul 20, 2022 - Use cautionMedical device
Getinge Usa Sales Inc recalls VOLISTA StandOP Surgical Light, Product Code/Part Numbers ARD568811901 VLT600SF AIM STP ARD568811911 VLT600SF AIM STP
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.
GetingeMay 6, 2022 - Use cautionMedical device
Getinge Usa Sales Inc recalls Flow-c Anesthesia System : intended for use in administering anesthesia while controlling the entire ventilation of
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.
GetingeMay 2, 2022 - Use cautionMedical device
Getinge Usa Sales Inc recalls Getinge CM320 WUWD Series Washer Disinfector-For use as a multi-chamber washer-disinfector for the washing,
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.
GetingeApr 13, 2022 - UnratedMedical device
Getinge Usa Sales Inc recalls Getinge 9100-Series Washer Disinfector models: 9120E, 9125E, 9127E, 9128E, 9122EW, 9128EW.
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.
GetingeApr 1, 2022 - Stop using nowMedical device
Getinge Usa Sales Inc recalls Vaporizer Sevoflurane Maquet Filling, Part No. 6886601 Component of the following systems: Product Code(s) UPN/UDI:
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.
GetingeDec 9, 2021
Getinge Usa Sales Inc recall questions
How many recalls has Getinge Usa Sales Inc had?
48 recalls from Getinge Usa Sales Inc are on record with U.S. safety agencies, from 2021–2025.
What is the most recent Getinge Usa Sales Inc recall?
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,, dated Jan 15, 2025. Every Getinge Usa Sales Inc recall is listed on this page, newest first.
Why are Getinge Usa Sales Inc products recalled?
The most common reasons on record: A potential for a light system to fall in the operating room. (15).
What should I do if I have a recalled Getinge Usa Sales Inc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Getinge Usa Sales Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.