Data Foundry

Medical device recalls 2024

Liberty Select Cycler — Class III medical device recall Z-0619-2024

Ongoing recall by Fresenius Medical Care Holdings, Inc., reported 2024-01-03, distributed nationwide. Affected Liberty Select cyclers may display an incorrect time stamp on the treatment data report sent to the c

Recall numberZ-0619-2024
Product typeMedical device
ClassificationClass III
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmFresenius Medical Care Holdings, Inc., Waltham, MA, United States
Recall initiated2023-10-24
Classified2023-12-26
Reported by FDA2024-01-03
DistributedNationwide (US)
Quantity149 us
UPC / GTIN / UDI-DI00840861102068
Serial numbersLC000539, LC001887, LC002257, LC002521, LC002956, LC002982, LC003341, LC003460, LC004607, LC004836, LC005140, LC006643, LC006834, LC007590, LC008971, LC009077, LC009410, LC010096, LC010282, LC010363, LC010500, LC010574, LC010607, LC011334, LC012490 and 124 more
Model numbersRTLR180111, RTLR180343

Product

Liberty Select Cycler, Model numbers RTLR180343 and RTLR180111

Reason for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0619-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.