# FDA recall D-0625-2020

> **Pharmedium Services, LLC** · Class III · drug recall initiated 2019-12-16.

## Product

NORepinephrine Bitartrate 8 mg added to 250 mL 5% Dextrose Injection USP (32 mcg per mL) Total Volume 258.00 mL Viaflex Bag, High Alert, Rx Only, PharMEDium Services LLC., 12620 W Airport Blvd #130 Sugar Land, TX 77478.

## Reason for recall

Subpotent Drug

## Distribution

Nationwide in the U.S.

## Key facts

- **Recall number:** D-0625-2020
- **Recalling firm:** Pharmedium Services, LLC
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-12-16
- **Report date:** 2020-01-01
- **Termination date:** 2021-02-09

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0625-2020

## Citation

> AI Analytics. FDA recall D-0625-2020. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/D-0625-2020. Source: US FDA. Licensed CC0.

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