# FDA recall D-1276-2014

> **Baxter Healthcare Corp.** · Class I · drug recall initiated 2014-02-11.

## Product

Dianeal PD-2 Peritoneal Dialysis Solution with 1.5% Dextrose, 6000 mL Ambu-Flex II container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Product Code L5B9710, NDC 0941-0411-11

## Reason for recall

Non-Sterility: Complaints of leaks and particulate matter identified as mold in the solution bag and the overpouch.

## Distribution

Nationwide.

## Key facts

- **Recall number:** D-1276-2014
- **Recalling firm:** Baxter Healthcare Corp.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-02-11
- **Report date:** 2014-05-07
- **Termination date:** 2015-07-22

- **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-1276-2014

## Citation

> AI Analytics. FDA recall D-1276-2014. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-1276-2014. Source: US FDA. Licensed CC0.

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