FDA Device recall Z-1311-2015
Alaris PC units, Model No. 8015
- FDA Device
- Class II
- terminated
- Published 2015-04-01
On 2015-04-01 the FDA classified a Class II recall of Alaris PC units, Model No. 8015 by Carefusion 303, citing careFusion is recalling the Alaris PC unit because of an error code. The error code may occur upon power on during the "Power-On Self Test" due to a keypad issue.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1311-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-03-12 |
| Published | 2015-04-01 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
Alaris PC units, Model No. 8015. Infusion pump.
Reason
CareFusion is recalling the Alaris PC unit because of an error code. The error code may occur upon power on during the "Power-On Self Test" due to a keypad issue.
Identifiers
| code_info | Serial No. 13874997 13875013 13875014 13875053 13875060 13875186 13875188 13875192 13875198 13875200 1387520…Serial No. 13874997 13875013 13875014 13875053 13875060 13875186 13875188 13875192 13875198 13875200 13875202 13875203 13875251 13875252 13875301 13875407 13875437 13875556 13875674 13875985 13876089 13876108 13876859 13877010 13877031 13877035 13877044 13877050 13877077 13877093 13877119 13877201 13877238 13877274 13877279 13877364 13877378 13877381 13877383 13877409 13877425 13877443 13877514 13877515 13877533 13877763 13877783 13877807 13877818 13877832 13877834 13877878 13877880 13877891 13877901 13877939 13877943 13877978 13877998 13877999 13878005 13878009 13878021 13878035 13878037 13878052 13878056 13878086 13878088 13878092 13878093 13878095 13878357 13878407 13878415 13878423 13878440 13878446 13878462 13878510 13878514 13878558 13878561 13878594 13878598 13878601 13878664 13879514 13879551 13879552 13879616 13879620 13879646 13879656 13879657 13879659 13879660 13879661 13879702 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1311-2015%22
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