The Hospira Symbiq Infusion System is intended for the delivery of… — Class II medical device recall Z-1847-2013
Terminated recall by Hospira Inc., reported 2013-08-07, distributed in AL, CA, CT, DE, FL, HI, IA, IL…. The devices secondary audio signal fails to activate.
| Recall number | Z-1847-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2013-02-04 |
| Classified | 2013-07-31 |
| Reported by FDA | 2013-08-07 |
| Terminated | 2016-11-07 |
| Distributed | AL, CA, CT, DE, FL, HI, IA, IL, IN, LA, MA, MD, ME, MI, MN, NC, NJ, NY, PA, SD, TX, WA |
| Quantity | 2,791 units |
| 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 and 475 more |
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 for recall
The devices secondary audio signal fails to activate.
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-1847-2013. 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.