FDA Device recall Z-0619-2024
Liberty Select Cycler, Model numbers RTLR180343 and RTLR180111
- FDA Device
- Class III
- ongoing
- Published 2024-01-03
On 2024-01-03 the FDA classified a Class III recall of Liberty Select Cycler, Model numbers RTLR180343 and RTLR180111 by Fresenius Medical Care Holdings, citing affected Liberty Select cyclers may display an incorrect time stamp on the treatment data report sent to the clinic.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0619-2024 |
| Classification | Class III |
| Status | ongoing |
| Initiated | 2023-10-24 |
| Published | 2024-01-03 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Fresenius Medical Care Holdings |
| Distribution | US |
Product
Liberty Select Cycler, Model numbers RTLR180343 and RTLR180111
Reason
Affected Liberty Select cyclers may display an incorrect time stamp on the treatment data report sent to the clinic.
Identifiers
| code_info | UDI-DI 00840861102068 Serial Numbers LC002956 LC102178 LC021724 LC107205 LC023197 LC021734 LC017434 LC108957 LC02206…UDI-DI 00840861102068 Serial Numbers LC002956 LC102178 LC021724 LC107205 LC023197 LC021734 LC017434 LC108957 LC022069 LC103031 LC006834 LC022218 LC017378 LC026229 LC022262 LC104084 LC005140 LC022616 LC019115 LC021388 LC024210 LC108220 LC020906 LC024377 LC023711 LC121383 LC025541 LC118552 LC010607 LC025545 LC015082 LC111682 LC026353 LC114222 LC105047 LC102656 LC113355 LC104022 LC103069 LC115736 LC109288 LC104268 LC016965 LC121349 LC104371 LC105964 LC003341 LC104630 LC016669 LC113929 LC105108 LC020357 LC111447 LC105656 LC003460 LC112030 LC105951 LC107408 LC025450 LC106453 LC109867 LC012490 LC107813 LC108319 LC106079 LC108527 LC106667 LC122086 LC108652 LC110922 LC119859 LC108929 LC022708 LC010574 LC108988 LC113343 LC118563 LC109815 LC000539 LC105216 LC110210 LC108637 LC103326 LC112490 LC103658 LC104946 LC112954 LC024150 LC017621 LC113920 LC017046 LC017185 LC114230 LC022051 LC010500 LC117266 LC001887 LC002982 LC117324 LC102332 LC106468 LC117470 LC007590 LC100108 LC118836 LC016220 LC1013 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0619-2024%22
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