Home / Recalls / Hospira Inc. / Z-2724-2016

Z-2724-2016 Class II Terminated

Recalled by Hospira Inc. — Lake Forest, IL

FDA device recall Z-2724-2016 was initiated by Hospira Inc. on Feb 6, 2013 and is designated Class II. 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. The recall status is terminated (terminated Nov 14, 2016). Affected quantity: 357,778 total.

Recall Details

Product Type: Devices
Report Date: Sep 14, 2016
Initiation Date: Feb 6, 2013
Termination Date: Nov 14, 2016
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 357,778 total

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.

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.

Distribution Pattern

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

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.

Source

Dataset: openFDA device recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for Z-2724-2016
openFDA file date: Oct 27, 2026
Loaded by RegDataLab: Oct 29, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

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