FDA Device recall Z-1074-2015
The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare environments
- FDA Device
- Class I
- terminated
- Published 2015-03-04
On 2015-03-04 the FDA classified a Class I recall of The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare environments by Hospira, citing one lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may fail to sound at all volume levels.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1074-2015 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2014-07-02 |
| Published | 2015-03-04 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Hospira |
| Distribution | AK, AL, AR, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY |
Product
The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare environments. It is a cassette based multi-function infusion system. The Plum A+ allows two lines in and one line out. The pump can be used for standard, piggyback, or concurrent delivery. Therapy modes include: Standard Infusions, Multistep Programming, Loading Dose, and Dose Calculation. The Plum A+ is designed to deliver parenteral, enteral, or epidural infusions over a broad range of infusion rates from multiple fluid container types. Each system includes a pumping module and an assortment of disposable IV sets, optional accessories, and an operator's manual.
Reason
One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may fail to sound at all volume levels.
Identifiers
| code_info | 1) List Number:11005: Serial Numbers: 18807410 , 18807428 , 18807439 , 18807459 , 18807511 , 18807523 , 18807578 , 16792228 , 16792250 |
|---|
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-1074-2015%22
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