FDA Device recall Z-0950-2017
Alaris Pump Module, Model No. 8100 and AIL sensor kits, P/N 147083-102 and P/N 49000221
- FDA Device
- Class I
- terminated
- Published 2017-01-25
On 2017-01-25 the FDA classified a Class I recall of Alaris Pump Module, Model No. 8100 and AIL sensor kits, P/N 147083-102 and P/N 49000221 by Carefusion 303, citing during an infusion, a false Air-in-Line (AIL) alarm would cause the infusion to be interrupted.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0950-2017 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2016-12-02 |
| Published | 2017-01-25 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
Alaris Pump Module, Model No. 8100 and AIL sensor kits, P/N 147083-102 and P/N 49000221. The Alaris Pump module is a large volume infusion pump offered under the Alaris System. The Alaris Pump module will deliver medication and fluids using IV administration sets for continuous or intermittent delivery through clinically acceptable routes of administration such as intravenous or epidural
Reason
During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion to be interrupted.
Identifiers
| code_info | All products manufactured or serviced in the time period October 2011 through June 2015. |
|---|
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-0950-2017%22
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