Potassium Chloride Injection 20 mEq — Class II drug recall D-0832-2016
Terminated recall by Hospira Inc., reported 2016-04-27, distributed nationwide. Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.
| Recall number | D-0832-2016 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2016-03-08 |
| Classified | 2016-04-21 |
| Reported by FDA | 2016-04-27 |
| Terminated | 2017-12-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | SG |
| Quantity | 81,888 bags |
| Reason classes | chemical contamination |
| NDC | 00409-7077-14 |
Product
Potassium Chloride Injection 20 mEq, 400 mEq/L, Packaged in 50 mL Bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7077-14
Reason for recall
Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.
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/D-0832-2016. 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.