FDA Device recall Z-1072-2015
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-1072-2015 |
| 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: 12391; Serial Numbers: 13840011 , 13840048 , 13840153 , 13840167 , 13840498 , 13840591 , 13840629…1) List Number: 12391; Serial Numbers: 13840011 , 13840048 , 13840153 , 13840167 , 13840498 , 13840591 , 13840629 , 13840640 , 13840943 , 13841068 , 13841130 , 13841271 , 13842284 , 13842383 , 13845291 , 13845368 , 13845404 , 13845429 , 13845450 , 13845495 , 13845510 , 13845560 , 13845599 , 13845686 , 13845697 , 13845701 , 13846352 , 13846723 , 13846727 , 13846788 , 13846801 , 13846803 , 13846804 , 13846807 , 13846826 , 13846827 , 13846847 , 13846852 , 13846862 , 13846877 , 13846878 , 13846902 , 13846971 , 13847066 , 13847663 , 13847677 , 13847698 , 13847702 , 13847707 , 13847719 , 13847777 , 13847802 , 13847804 , 13847805 , 13847812 , 13847815 , 13847836 , 13847838 , 13847840 , 13847841 , 13847847 , 13847873 , 13847887 , 13847893 , 13847898 , 13847901 , 13847905 , 13847907 , 13847916 , 13847942 , 13847947 , 13847956 , 13847960 , 13847965 , 13847973 , 13847984 , 13847988 , 13848031 , 13848043 , 13848044 , 1 |
|---|
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-1072-2015%22
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