Hospira Inc. recalls The Symbiq infusion pump is a device used in a health care facility to pump fluids into a patient in a controlled manne…

Recall date

December 22, 2015

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0863-2016

FDA classification

Class II

Brand / firm

Hospira Inc.

Sold / distributed

U.S. consignees nationwide.*** Foreign consignees in: Canada.

Why it was recalled

Potential for the Symbiq pole clamp assemblies to be missing the rubber stop pad.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

The Symbiq infusion pump is a device used in a health care facility to pump fluids into a patient in a controlled manner. It is intended primarily for use in the hospital setting and can be used in other acute and non-acute areas, such as, but not limited to, Nursing Homes, Mobile Intensive Care, Ambulatory Infusion, Centers, Hospice, Sub acute facilities, Outpatient/Surgical Centers, Long-term Care, Urgent Care, Transport, and Physician Offices.