FDA Device recall Z-2700-2017
Alaris Pump Module model 8100
- FDA Device
- Class II
- terminated
- Published 2017-07-19
On 2017-07-19 the FDA classified a Class II recall of Alaris Pump Module model 8100 by Carefusion 303, citing there is a potential risk that could cause unintended flow in the older, centered sear door latch design in the Alaris Pump module model 8100.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2700-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-06-12 |
| Published | 2017-07-19 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Carefusion 303 |
| Distribution | n/a |
Product
Alaris Pump Module model 8100
Reason
There is a potential risk that could cause unintended flow in the older, centered sear door latch design in the Alaris Pump module model 8100.
Identifiers
| code_info | Notification will be distributed to all Alaris Pumps customers with pumps manufactured between June 2002 through June 2004. |
|---|
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-2700-2017%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.