Data Foundry

Medical device recalls 2013

*** 1) SYMBIQ One-Channel Infuser — Class II medical device recall Z-0372-2014

Terminated recall by Hospira Inc., reported 2013-11-27, distributed in KY, MN, ND, NJ, NY, PA, SD. Hospira shipped the incorrect replaceable battery pack (Part No: HSP3566-E10) instead of the correct E09 batte

Recall numberZ-0372-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmHospira Inc., Lake Forest, IL, United States
Recall initiated2013-08-28
Classified2013-11-20
Reported by FDA2013-11-27
Terminated2016-11-07
DistributedKY, MN, ND, NJ, NY, PA, SD
Quantity59 batteries
Model numbersHSP3566-E09, HSP3566-E10

Product

*** 1) SYMBIQ One-Channel Infuser; *** 2) SYMBIQ Two-Channel Infuser; *** E09 batteries can be identified by the "E09" that is printed beneath the bar code and at the end of the serial number along the bottom of the label found on each battery; *** E10 batteries can be identified by the "E10" that is printed beneath the bar code and at the end of the serial number along the bottom of the label found on each battery. Symbiq is a general-purpose infuser designed to deliver fluids, solutions, medications, agents, nutritionals, electrolytes, blood and blood products for parenteral, enteral, intra-arterial, subcutaneous, or irrigation routes of administration.

Reason for recall

Hospira shipped the incorrect replaceable battery pack (Part No: HSP3566-E10) instead of the correct E09 battery pack (Part No. HSP3566-E09) for the Symbiq Single and Dual Channel Infusers.

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-0372-2014. 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.