# FDA recall D-1825-2015

> **Pharmedium Services, LLC** · Class I · drug recall initiated 2015-01-28.

## Product

Fentanyl Citrate, 5 mcg per mL (1,250 mcg per 250 mL), 250 mL total volume in a 250 mL LifeCare bag in Sodium Chloride 0.9%, IV Use Only, Rx only, PharMEDium Services, LLC, 6100 Global Drive, Memphis, TN  36141, NDC# 61553-107-50

## Reason for recall

Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter (human hair).

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1825-2015
- **Recalling firm:** Pharmedium Services, LLC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-01-28
- **Report date:** 2015-09-30
- **Termination date:** 2017-01-27

- **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-1825-2015

## Citation

> AI Analytics. FDA recall D-1825-2015. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-1825-2015. Source: US FDA. Licensed CC0.

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