# FDA recall D-0132-2018

> **Pharmedium Services, LLC** · Class III · drug recall initiated 2017-09-26.

## Product

HYDROmorphone HCl in 0.9% Sodium Chloride Injection, 1 mL Total Volume 1 mg per mL, For IV Use Only, Rx Only, Compounded by: PharMEDium Services LLC. 913 N Davis Ave Cleveland, MS 38732, NDC# 61553-165-78

## Reason for recall

Labeling: Incorrect or Missing Lot and/or Exp. Date

## Distribution

Nationwide.

## Key facts

- **Recall number:** D-0132-2018
- **Recalling firm:** Pharmedium Services, LLC
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-09-26
- **Report date:** 2018-01-03
- **Termination date:** 2020-05-19

- **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-0132-2018

## Citation

> AI Analytics. FDA recall D-0132-2018. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-0132-2018. Source: US FDA. Licensed CC0.

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