FDA Device recall Z-0863-2016

The Symbiq infusion pump is a device used in a health care facility to pump fluids into a patient in a controlled manner

FDA Device
Class II
terminated
Published 2016-03-02

On 2016-03-02 the FDA classified a Class II recall of The Symbiq infusion pump is a device used in a health care facility to pump fluids into a patient in a controlled manner by Hospira, citing potential for the Symbiq pole clamp assemblies to be missing the rubber stop pad.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0863-2016
Classification	Class II
Status	terminated
Initiated	2015-12-22
Published	2016-03-02
Last updated	2026-09-13 11:54 UTC
Company	Hospira
Distribution	US

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.

Reason

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

Identifiers

code_info	Lot Code 16026 &16027 with the following serial numbers: 14339221, 14339224, 14339232, 14339261, 14339275, 14339296, 14… Lot Code 16026 &16027 with the following serial numbers: 14339221, 14339224, 14339232, 14339261, 14339275, 14339296, 14339308, 14339321, 14339335, 14339349, 14339353, 14339357, 14339371, 14339372, 14339378, 14339387, 14339391, 14339396, 14339401, 14339504, 14339515, 14339553, 14339710, 14339719, 14339725, 14339733, 14339738, 14339742, 14339748, 14339761, 14339769, 14339771, 14339799, 14339815, 14339822, 14339851, 14339887, 14339888, 14339904, 14339913, 14339964, 14339989, 14339998, 14339999, 14340001, 14340014, 14340041, 14340042, 14340069, 14340070, 14340071, 14340094, 14340096, 14340110, 14340117, 14340119, 14340120, 14340122, 14340123, 14340124, 14340127, 14340133, 14340134, 14340138, 14340143, 14340144, 14340146, 14340147, 14340153, 14340154, 14340158, 14340163, 14340176, 14340182, 14340184, 14340186, 14340188, 14340200, 14340209, 14340211, 14340214, 14340225, 14340227, 14340232, 14340245, 14340248, 14340251, 14340253, 14340255, 14340263, 14340264, 14340268, 14340274, 14340276, 143

code_info

Lot Code 16026 &16027 with the following serial numbers: 14339221, 14339224, 14339232, 14339261, 14339275, 14339296, 14…

Lot Code 16026 &16027 with the following serial numbers: 14339221, 14339224, 14339232, 14339261, 14339275, 14339296, 14339308, 14339321, 14339335, 14339349, 14339353, 14339357, 14339371, 14339372, 14339378, 14339387, 14339391, 14339396, 14339401, 14339504, 14339515, 14339553, 14339710, 14339719, 14339725, 14339733, 14339738, 14339742, 14339748, 14339761, 14339769, 14339771, 14339799, 14339815, 14339822, 14339851, 14339887, 14339888, 14339904, 14339913, 14339964, 14339989, 14339998, 14339999, 14340001, 14340014, 14340041, 14340042, 14340069, 14340070, 14340071, 14340094, 14340096, 14340110, 14340117, 14340119, 14340120, 14340122, 14340123, 14340124, 14340127, 14340133, 14340134, 14340138, 14340143, 14340144, 14340146, 14340147, 14340153, 14340154, 14340158, 14340163, 14340176, 14340182, 14340184, 14340186, 14340188, 14340200, 14340209, 14340211, 14340214, 14340225, 14340227, 14340232, 14340245, 14340248, 14340251, 14340253, 14340255, 14340263, 14340264, 14340268, 14340274, 14340276, 143

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0863-2016%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.