FDA recall record

Fresenius Medical Care Holdings Liberty Select Cycler, Model numbers RTLR180343 and recall — FDA Z-0619-2024

Affected Liberty Select cyclers may display an incorrect time stamp on the treatment data report sent to the clinic.

Class IIIclassification
Z-0619-2024official record ID
Jan 3, 2024report date

Recall record at a glance

Official recordZ-0619-2024
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusOngoing
Recalling firmFresenius Medical Care Holdings, Inc.
Report dateJan 3, 2024
Recall initiation dateOct 24, 2023
Quantity149 US
LocationWaltham, MA, United States

Official product description

Liberty Select Cycler, Model numbers RTLR180343 and RTLR180111

Why the product was recalled

Affected Liberty Select cyclers may display an incorrect time stamp on the treatment data report sent to the clinic.

Distribution information

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.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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