Getinge Group Logistics America, LLC recalls
Every recall we track for Getinge Group Logistics America, LLC — 4 in all, from 2020–2021 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
4 recalls since 2017.
All FDA recall records for Getinge Group Logistics America, LLC 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 | 1 | 1 | 0 | 2 |
| 2021 | 0 | 2 | 0 | 0 | 2 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Getinge Group Logistics America, LLC 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 Group Logistics America, LLC recalls
4 shown- Use cautionMedical device
Getinge Group Logistics America, LLC recalls Operating Table System
Getinge recalls specific operating table models due to potential hydraulic leakage causing unintended table movements that may delay surgery. Affected units include part numbers 118001A0 through 118001D0.
GetingeFeb 11, 2021 - Use cautionMedical device
Getinge Group Logistics America, LLC recalls Anesthesia gas-machine - Product Usage: intended for use in administering anesthesia while controlling the entire
Getinge recalls Flow i anesthesia machines with FiCO2 value errors or system check failures. Affected models include Flow i C20, C30, C40 and Flow c systems with specific serial numbers. Users should contact Getinge for remedy.
GetingeJan 29, 2021 - Use cautionMedical device
Getinge Group Logistics America, LLC recalls Getinge CM320 Series Washer Disinfector - Product Usage: A multi chamber washer disinfector intended for washing,
Getinge recalls CM320 Series washer disinfectors due to potential hose connections breaking, causing water leaks or sprays that could lead to burns or procedural delays. Affected units have specific serial numbers and product codes.
GetingeDec 21, 2020 - Lower riskMedical device
Getinge Group Logistics America, LLC recalls Servo-i Ventilator, Part No. 6487800, UDI Code 07325710000823 - Product Usage: intended for general and critical
Getinge recalls Servo-i Ventilators with specific serial numbers due to a potentially shorter nebulizer connector that may cause difficulty installing the Aeroneb Nebulizer module. Affected units can be identified by serial numbers listed in the recall notice.
GetingeSep 17, 2020
Getinge Group Logistics America, LLC recall questions
How many recalls has Getinge Group Logistics America, LLC had?
4 recalls from Getinge Group Logistics America, LLC are on record with U.S. safety agencies, from 2020–2021.
What is the most recent Getinge Group Logistics America, LLC recall?
Getinge Group Logistics America, LLC recalls Operating Table System, dated Feb 11, 2021. Every Getinge Group Logistics America, LLC recall is listed on this page, newest first.
What should I do if I have a recalled Getinge Group Logistics America, LLC 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 Group Logistics America, LLC 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.