# FDA recall D-1141-2023

> **Baxter Healthcare Corporation** · Class II · drug recall initiated 2023-08-11.

## Product

Dianeal PD-2 Peritonial Dialysis Solution with 1.5% Dextrose, 5000 mL AMBU-FLEX ll Container with yellow pull ring, Rx Only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA Product code L5B5193 NDC 0941-0411-07

## Reason for recall

Lack of Assurance of Sterility: Potential presence of leaks originating from the Luer component.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-1141-2023
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2023-08-11
- **Report date:** 2023-09-06
- **Termination date:** 2024-07-16

- **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-1141-2023

## Citation

> AI Analytics. FDA recall D-1141-2023. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-1141-2023. Source: US FDA. Licensed CC0.

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