Hospira Inc.: Medical Device Recall in 2016 - (Recall #: Z-2724-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Plum A+ Infusion Pump. List Number 11973. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained, microprocessor based infusion devices.

Product Classification:

Class II

Date Initiated: February 6, 2013

Date Posted: September 14, 2016

Recall Number: Z-2724-2016

Event ID: 64261

Reason for Recall:

The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.

Status: Terminated

Product Quantity: 357,778 total

Code Information:

List Number 11973. Serial numbers: 12570148, 12570150, 12570154, 12570163, 12570170, 12570177, 12570204, 12570211, 12570212, 12570255, 12570270, 12570319, 12570359, 12570385, 12570413, 12570425, 12570455, 12570487, 12570662, 12570695, 12570854, 12570915, 12571080, 12571243, 12571437, 12571631, 12571692, 12571776, 12571826, 12571835, 12571837, 12571842, 12571877, 12571880, 12571886, 12572317, 12572369, 12572586, 12572909, 12573547, 12573567, 12573837, 12573990, 12574424, 12574501, 12574524, 12574556, 12574599, 12574619, 12574731, 12574749, 12574853, 12574858, 12574860, 12574865, 12574961, 12575626, 12575698, 12575886, 12576125, 12576443, 12576485, 12576518, 12576593, 12576609, 12576710, 12576722, 12577271, 12577685, 12578856, 12579183.

Distribution Pattern:

United States nationwide distribution including PR, and USVI. Costa Rica, Turks and Caicos, and Dominican Republic.

Voluntary or Mandated:

Voluntary: Firm initiated