FDA Device recall Z-1847-2013
The Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents, nutritionals, electrolytes, blood and…
- FDA Device
- Class II
- terminated
- Published 2013-08-07
On 2013-08-07 the FDA classified a Class II recall of The Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents, nutritionals, electrolytes, blood and… by Hospira, citing the devices secondary audio signal fails to activate.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1847-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-02-04 |
| Published | 2013-08-07 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Hospira |
| Distribution | AL, CA, CT, DE, FL, HI, IA, IL, IN, LA, MA, MD, ME, MI, MN, NC, NJ, NY, PA, SD, TX, WA |
Product
The Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents, nutritionals, electrolytes, blood and blood products via parenteral, enteral, intravenous, intra-arterial, subcutaneous, epidural, or irrigation routes of administration.
Reason
The devices secondary audio signal fails to activate.
Identifiers
| code_info | *** 1) List Number 16206, Serial Numbers: 0017234975 , 0017234978 , 0017234979 , 0017234980 , 0017234981 , 0017234…*** 1) List Number 16206, Serial Numbers: 0017234975 , 0017234978 , 0017234979 , 0017234980 , 0017234981 , 0017234982 , 0017234983 , 0017234984 , 0017234985 , 0017234986 , 0017234988 , 0017234991 , 0017234992 , 0017234993 , 0017234994 , 0017234995 , 0017234996 , 0017234997 , 0017234998 , 0017234999 , 0017235001 , 0017235002 , 0017235003 , 0017235004 , 0017235005 , 0017235006 , 0017235007 , 0017235008 , 0017235009 , 0017235010 , 0017235011 , 0017235014 , 0017235015 , 0017235016 , 0017235017 , 0017235018 , 0017235019 , 0017235020 , 0017235021 , 0017235022 , 0017235023 , 0017235024 , 0017235025 , 0017235026 , 0017235028 , 0017235029 , 0017235030 , 0017235031 , 0017235032 , 0017235033 , 0017235034 , 0017235035 , 0017235036 , 0017235037 , 0017235038 , 0017235039 , 0017235041 , 0017235042 , 0017235043 , 0017235044 , 0017235045 , 0017235046 , 0017235048 , 0017235049 , 0017235050 , 0017235051 , 0017235052 , 0017235053 , 001723 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1847-2013%22
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