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 manner

Recalled March 2, 2016 · FDA recall Z-0863-2016 · Hospira

Hazard

Potential for the Symbiq pole clamp assemblies to be missing the rubber stop pad. · FDA Class II

Units

6634 units.

Sold at

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

Description

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

Product

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.

Manufacturer(s)

Hospira Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →