FDA Drug recall D-0832-2016
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
- FDA Drug
- Class II
- terminated
- Published 2016-04-27
On 2016-04-27 the FDA classified a Class II recall of 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 by Hospira, citing chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0832-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-03-08 |
| Published | 2016-04-27 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Hospira |
| Distribution | US |
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
Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.
Identifiers
| code_info | Lo# 53-006-JT, Exp 11/16 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0832-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.