FDA Device recall Z-1179-2016
Alaris Pump VersaSafe Infusion Set, Model No. 2122-0007
- FDA Device
- Class II
- terminated
- Published 2016-03-23
On 2016-03-23 the FDA classified a Class II recall of Alaris Pump VersaSafe Infusion Set, Model No. 2122-0007 by Carefusion 303, citing careFusion is recalling the Alaris VersaSafe Infusion Set because of separation and/or leakages at the VersaSafe split septum port and tubing may lead to leakage of the administra….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1179-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-02-15 |
| Published | 2016-03-23 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Carefusion 303 |
| Distribution | MI |
Product
Alaris Pump VersaSafe Infusion Set, Model No. 2122-0007
Reason
CareFusion is recalling the Alaris VersaSafe Infusion Set because of separation and/or leakages at the VersaSafe split septum port and tubing may lead to leakage of the administration set.
Identifiers
| code_info | Lot No. 13085603 |
|---|
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-1179-2016%22
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