Data Foundry

Medical device recalls 2016

The Symbiq infusion pump is a device used in a health care facility… — Class II medical device recall Z-0863-2016

Terminated recall by Hospira Inc., reported 2016-03-02, distributed nationwide. Potential for the Symbiq pole clamp assemblies to be missing the rubber stop pad.

Recall numberZ-0863-2016
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmHospira Inc., Lake Forest, IL, United States
Recall initiated2015-12-22
Classified2016-02-23
Reported by FDA2016-03-02
Terminated2016-11-28
DistributedNationwide (US)
Countries outside the USCA
Quantity6,634 units
Lot numbers16026, 16027
Serial numbers14339221, 14339224, 14339232, 14339261, 14339275, 14339296, 14339308, 14339321, 14339335, 14339349, 14339353, 14339357, 14339371, 14339372, 14339378, 14339387, 14339391, 14339396, 14339401, 14339504, 14339515, 14339553, 14339710, 14339719, 14339725 and 475 more

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 for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0863-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.