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.
Reported: March 2, 2016 Initiated: December 22, 2015 #Z-0863-2016
Product Description
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.
Reason for Recall
Potential for the Symbiq pole clamp assemblies to be missing the rubber stop pad.
Details
- Recalling Firm
- Hospira Inc.
- Units Affected
- 6634 units.
- Distribution
- U.S. consignees nationwide.*** Foreign consignees in: Canada.
- Location
- Lake Forest, IL
Frequently Asked Questions
What product 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.. Recalled by Hospira Inc.. Units affected: 6634 units..
Why was this product recalled? ▼
Potential for the Symbiq pole clamp assemblies to be missing the rubber stop pad.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 2, 2016. Severity: Moderate. Recall number: Z-0863-2016.
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