Potassium Chloride Injection — Class II drug recall D-1606-2014
Terminated recall by Baxter Healthcare Corp, reported 2014-10-01, distributed nationwide. Correct Labeled Product Mispack: Shipping cartons labeled as containing Potassium Chloride injection actually
| Recall number | D-1606-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corp, Deerfield, IL, United States |
| Recall initiated | 2014-09-08 |
| Classified | 2014-09-23 |
| Reported by FDA | 2014-10-01 |
| Terminated | 2016-09-27 |
| Distributed | Nationwide (US) |
| Quantity | 148,632 bags |
| Reason classes | labeling |
| NDC | 00338-0703, 00338-0703-41, 00338-0703-48, 00338-0705, 00338-0705-41, 00338-0705-48, 00338-0709, 00338-0709-48 |
| Lot numbers | P318220 |
| Expiration dates | 2015-05-31 |
Product
Potassium Chloride Injection, 10 mEq per 100 mL, Highly Concentrated (100 mEq/L), 100 mL Sterile single dose container bags, Rx only, Baxter USA, product code 2B0826, NDC 0338-0709-48.
Reason for recall
Correct Labeled Product Mispack: Shipping cartons labeled as containing Potassium Chloride injection actually contained bags labeled and containing Gentamicin Sulfate injection inside.
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-1606-2014. 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.