FDA Device recall Z-2671-2017
Alaris PC Unit, Model 8015
- FDA Device
- Class II
- terminated
- Published 2017-07-12
On 2017-07-12 the FDA classified a Class II recall of Alaris PC Unit, Model 8015 by Carefusion 303, citing BD initiated the recall of Alaris PC unit model 8015 after the firm identified five scenarios which can result in the occurrence of Systems Error Code 255-16-275 and can potential….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2671-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-06-12 |
| Published | 2017-07-12 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
Alaris PC Unit, Model 8015
Reason
BD initiated the recall of Alaris PC unit model 8015 after the firm identified five scenarios which can result in the occurrence of Systems Error Code 255-16-275 and can potentially result in interrupted infusions.
Identifiers
| code_info | Notification will be distributed to all Alaris PC Unit model 8015 customers with software versions greater than 9.12. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2671-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.