FDA Device recall Z-1073-2015

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-1073-2015
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: 20678: Serial Numbers: 15867001 , 15938721 , 15900791 , 15900971 , 15901051 , 15901101 , 15901301… 1) List Number: 20678: Serial Numbers: 15867001 , 15938721 , 15900791 , 15900971 , 15901051 , 15901101 , 15901301 , 15902021 , 15886121 , 15886191 , 15886201 , 15886331 , 15887441 , 15887451 , 15887501 , 15887541 , 15887551 , 15887561 , 15887571 , 15887591 , 15887601 , 15887621 , 15887721 , 15887781 , 15887801 , 15887811 , 15887841 , 15887851 , 15887861 , 15909721 , 15910521 , 15910551 , 15911281 , 15911441 , 15911501 , 15911631 , 15922951 , 15926291 , 15926731 , 15926961 , 15927281 , 15927621 , 15927731 , 15927781 , 15928041 , 15928061 , 15928131 , 15928171 , 15928221 , 15928231 , 15928291 , 15928951 , 15929051 , 15929151 , 15929351 , 15929531 , 15929901 , 15930141 , 15930191 , 15930341 , 15930351 , 15930641 , 15930691 , 15930711 , 15931171 , 15933301 , 15933501 , 15933821 , 15933941 , 15933991 , 15934001 , 15934171 , 15934261 , 15934681 , 15934711 , 15934841 , 15934891 , 15935011 , 15935071 , 15935141 , 1

code_info

1) List Number: 20678: Serial Numbers: 15867001 , 15938721 , 15900791 , 15900971 , 15901051 , 15901101 , 15901301…

1) List Number: 20678: Serial Numbers: 15867001 , 15938721 , 15900791 , 15900971 , 15901051 , 15901101 , 15901301 , 15902021 , 15886121 , 15886191 , 15886201 , 15886331 , 15887441 , 15887451 , 15887501 , 15887541 , 15887551 , 15887561 , 15887571 , 15887591 , 15887601 , 15887621 , 15887721 , 15887781 , 15887801 , 15887811 , 15887841 , 15887851 , 15887861 , 15909721 , 15910521 , 15910551 , 15911281 , 15911441 , 15911501 , 15911631 , 15922951 , 15926291 , 15926731 , 15926961 , 15927281 , 15927621 , 15927731 , 15927781 , 15928041 , 15928061 , 15928131 , 15928171 , 15928221 , 15928231 , 15928291 , 15928951 , 15929051 , 15929151 , 15929351 , 15929531 , 15929901 , 15930141 , 15930191 , 15930341 , 15930351 , 15930641 , 15930691 , 15930711 , 15931171 , 15933301 , 15933501 , 15933821 , 15933941 , 15933991 , 15934001 , 15934171 , 15934261 , 15934681 , 15934711 , 15934841 , 15934891 , 15935011 , 15935071 , 15935141 , 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-1073-2015%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.