# FDA recall D-1690-2012

> **Baxter Healthcare Corp.** · Class II · drug recall initiated 2012-09-21.

## Product

Lactated Ringer's Injection USP, packaged in a) 250 mL AVIVA Container, product code 6E2322B, NDC 0338-6307-02; b) 500 mL AVIVA Container, product code 6E2323, NDC 0338-6307-03; Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA

## Reason for recall

Chemical Contamination: The IV solutions were packaged in AVIVA containers which may contain trace levels of cumene hydroperoxide (CHP).

## Distribution

Nationwide and Puerto Rico

## Key facts

- **Recall number:** D-1690-2012
- **Recalling firm:** Baxter Healthcare Corp.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-09-21
- **Report date:** 2012-10-03
- **Termination date:** 2015-05-04

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1690-2012

## Citation

> AI Analytics. FDA recall D-1690-2012. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-1690-2012. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*