# FDA recall D-0777-2016

> **Pharmedium Services, LLC** · Class III · drug recall initiated 2015-12-31.

## Product

NORepinephrine Bitartrate, 4 mg (16 mcg/mL) added to 250 mL 0.9% Sodium Chloride Injection USP, in 250 mL Viaflex Bag, Rx only, PharMEDium Services, LLC, Sugar Land, TX NDC 61553-134-61

## Reason for recall

Subpotent Drug; confirmed results by FDA analysis after customer complaints of discoloration

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0777-2016
- **Recalling firm:** Pharmedium Services, LLC
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-12-31
- **Report date:** 2016-03-23
- **Termination date:** 2016-04-06

- **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-0777-2016

## Citation

> AI Analytics. FDA recall D-0777-2016. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/D-0777-2016. Source: US FDA. Licensed CC0.

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