The Recall Desk
HighFDA (Devices)·Z-0207-2014·Announced 2013-11-20

Hospira Recalls Plum A+ Infusion Pumps Due to Pressure Sensor Calibration Drift

Hospira is recalling 182,970 Plum A+ Infusion Pumps because pressure sensor calibration drift may cause false alarms or missed occlusions.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall is classified as FDA Class II, and the defect involves a risk-of-harm product (infusion pump) where injury has not yet been reported, fitting the criteria for a High severity score.

Plain-English summary

Hospira Inc. is recalling 182,970 units of the Plum A+ Infusion Pump (List Number 12391) due to reports of distal pressure sensor calibration drift. The affected devices are a multipurpose family of infusion systems used for precise delivery of multiple therapies across the general spectrum of clinical care.

The calibration drift may result in the display of specific error codes during setup or infusion, including E180/N180, E181/N181, E186/N186, E187/N187, or E346. Additionally, the drift may cause users to experience false distal occlusion alarms or distal occlusions that may not be properly detected. The source text does not report any specific injuries or illnesses associated with this defect.

The affected units were distributed nationwide in the United States, including all 50 states, the District of Columbia, Puerto Rico, and the U.S. Virgin Islands, as well as in Croatia, the Dominican Republic, and Turks and Caicos. Specific serial numbers are listed in the official recall documentation. Users should check their device serial numbers against the provided list and contact Hospira for further instructions.

The recalled product

Product
Plum A+ Infusion Pump; List Number: 12391; Product Usage: The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care
Manufacturer
Hospira Inc.
Category
Medical Device — Infusion Pump
Hazard

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (20)

  • List No. 12391
  • Serial Numbers: 13840001
  • 13840002
  • 13840003
  • 13840004
  • 13840005
  • 13840006
  • 13840007
  • 13840008
  • 13840009
  • 13840010
  • 13840011
  • 13840012
  • 13840013
  • 13840014
  • 13840015
  • 13840016
  • 13840017
  • 13840018
  • 13840019

Distribution

Distributed nationwide across the United States.

The notice also names 51 states specifically:

Part of a larger recall action

This product is one of 7 recalled by Hospira Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 7 products in this recall →

Related recalls

Same manufacturer · Hospira Inc.

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Same hazard · calibration drift

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