# FDA recall D-1606-2014

> **Baxter Healthcare Corp** · Class II · drug recall initiated 2014-09-08.

## 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.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1606-2014
- **Recalling firm:** Baxter Healthcare Corp
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-09-08
- **Report date:** 2014-10-01
- **Termination date:** 2016-09-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1606-2014

## Citation

> AI Analytics. FDA recall D-1606-2014. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-1606-2014. Source: US FDA. Licensed CC0.

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