# FDA recall D-1348-2022

> **Baxter Healthcare Corporation** · Class II · drug recall initiated 2022-08-04.

## Product

Acetaminophen Injection, 10 mg/mL, 1,000 mg/100 mL, 100 mL VIAFLO container bag, Single Dose Container, For Intravenous Use Only, Rx Only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA; NDC 36000-306-60

## Reason for recall

Temperature Abuse: Product distributed in refrigerated trucks with labels attached to pallets indicating "Refrigerate Upon Arrival", however product is labeled to be stored in a controlled room temperature environment.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-1348-2022
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-08-04
- **Report date:** 2022-08-24
- **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-1348-2022

## Citation

> AI Analytics. FDA recall D-1348-2022. Retrieved 2026-07-10 from https://api.ai-analytics.org/recall/D-1348-2022. Source: US FDA. Licensed CC0.

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