# FDA recall D-0596-2025

> **Baxter Healthcare Corporation** · Class II · drug recall initiated 2025-08-20.

## Product

Acetaminophen Injection 1000 mg/100 mL (10 mg/mL), packaged in 100 mL Viaflo container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Made in Ireland, NDC 36000-306-60.

## Reason for recall

Discoloration

## Distribution

U.S.A. Nationwide

## Key facts

- **Recall number:** D-0596-2025
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2025-08-20
- **Report date:** 2025-09-03

- **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-0596-2025

## Citation

> AI Analytics. FDA recall D-0596-2025. Retrieved 2026-07-31 from https://api.ai-analytics.org/recall/D-0596-2025. Source: US FDA. Licensed CC0.

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