FDA Device recall Z-1793-2020
PREVI Isola Insrument and PREVI Isola Printer spares PSUs (power supply units), P1028888-001 PSU (used in Zebra LP2824 Plus printers) PSUs…
- FDA Device
- Class II
- terminated
- Published 2020-04-29
On 2020-04-29 the FDA classified a Class II recall of PREVI Isola Insrument and PREVI Isola Printer spares PSUs (power supply units), P1028888-001 PSU (used in Zebra LP2824 Plus printers) PSUs… by Biomerieux, citing the recall has been initiated due to potential for overheating or a fire hazard associated with the Zebra LP2824 Plus printer PSU (power supply unit) located within the PREVI Isol….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1793-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-01-24 |
| Published | 2020-04-29 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Biomerieux |
| Distribution | US |
Product
PREVI Isola Insrument and PREVI Isola Printer spares PSUs (power supply units), P1028888-001 PSU (used in Zebra LP2824 Plus printers) PSUs with the following date code; 0639XX through 1253XX (YYWWXX, where YY=Year, and WW=week).
Reason
The recall has been initiated due to potential for overheating or a fire hazard associated with the Zebra LP2824 Plus printer PSU (power supply unit) located within the PREVI Isola instrument.
Identifiers
| code_info | Instrument Serial Number AS180-00028 1035196 AS180-00067 1007580 AS180-00084 2055833 AS180-00105 2025461 AS18…Instrument Serial Number AS180-00028 1035196 AS180-00067 1007580 AS180-00084 2055833 AS180-00105 2025461 AS180-00138 2025461 AS180-00179 1039938 AS180-00217 1033454 AS180-00248 1029262 AS180-00278 1031886 AS180-00300 1033400 AS180-00306 1034034 AS180-00326 1034190 AS180-00336 1041241 AS180-00339 2054793 AS180-00357 2055775 AS180-00381 1073849 AS180-00385 1054234 AS180-00398 1052053 AS180-00402 2055620 AS180-00405 1063739 AS180-00418 1042188 AS180-00420 1040343 AS180-00428 1030890 AS180-00453 1031472 AS180-00468 1043640 AS180-00476 1029272 AS180-00478 1053432 AS180-00479 1011691 AS180-00480 5001554 AS180-00481 1039588 AS180-00482 1034363 AS180-00483 1029990 AS180-00484 1049298 AS180-00485 AU01 AS180-00486 1047965 AS180-00487 1074074 AS180-00488 1000283 AS180-00489 1035594 AS180-00490 1047965 AS180-00491 1035549 AS180-00492 1070878 AS180-00493 1090075 AS180-00494 1039290 AS180-00495 1029148 AS180-00 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1793-2020%22
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