Fresenius Liberty Select Cycler: Incorrect Time Stamp on Treatment Reports
Fresenius Medical Care recalls Liberty Select cyclers with model numbers RTLR180343 and RTLR180111 due to potential incorrect time stamps on treatment reports sent to clinics. Affected units may require correction to ensure accurate patient data.
Lower-risk recall
Affected Liberty Select cyclers may display an incorrect time stamp on the treatment data report sent to the clinic.
Contact the company
What happened, in plain English
Fresenius Medical Care is recalling Liberty Select cyclers with specific model numbers because they may show incorrect time stamps on treatment reports sent to clinics. This could lead to inaccurate patient data being recorded, which might affect treatment timing and safety. Read more at govinfonow.com/recall/57018-fresenius-liberty-select-cycler-incorrect-time-stamp-on-treatment-reports.
Source Summary by GovInfoNow · govinfonow.com/recall/57018-fresenius-liberty-select-cycler-incorrect-time-stamp-on-treatment-reports · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0619-2024
Cite this page
“Fresenius Liberty Select Cycler: Incorrect Time Stamp on Treatment Reports.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/57018-fresenius-liberty-select-cycler-incorrect-time-stamp-on-treatment-reports. Based on FDA recall #Z-0619-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0619-2024%22&limit=1).
Why it’s dangerous
The device may display an incorrect time stamp on the treatment data report sent to the clinic. This could result in inaccurate patient data being recorded, potentially affecting treatment timing and safety. However, the hazard does not involve immediate physical harm or malfunction.
Who’s affected
Patients using the Liberty Select Cycler with model numbers RTLR180343 or RTLR180111 are likely affected. Healthcare providers who send treatment reports from these devices are at the highest risk of inaccurate data.
How to tell if you have this one
Check for model numbers RTLR180343 or RTLR180111 on the device. The serial numbers listed in the recall notice include LC002956 and other specific numbers.
- Brand
Fresenius Medical Care- Category
Medical device
What to do — step by step
Check Device Model
Identify the model number on your Liberty Select Cycler to see if it is RTLR180343 or RTLR180111.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 20 states.
FDA distribution: “US Nationwide distribution in the states of AL, CA, FL, IL, IN, LA, MI, MO, MT, NC, NJ, NV, OH, OK, OR, PA, SC, TN, TX, VA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, California, Florida, Illinois, Indiana, Louisiana, Michigan, Missouri, Montana, Nevada, New Jersey, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia.
Recall timeline
FDA published this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-0619-2024 (October 24, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0619-2024 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.