# FDA recall D-0080-2018

> **PharMEDium Services, LLC.** · Class II · drug recall initiated 2017-10-13.

## Product

Hydromorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride Injection 1 mL, packaged in syringes, Rx Only , PharMEDium Services, LLC. 913 N. Davis Ave Cleveland, MS 38732, NDC 61553-352-40

## Reason for recall

Superpotent drug: out of specification result for potency

## Distribution

CA, IL

## Key facts

- **Recall number:** D-0080-2018
- **Recalling firm:** PharMEDium Services, LLC.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-10-13
- **Report date:** 2017-11-22
- **Termination date:** 2020-01-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Memphis, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0080-2018

## Citation

> AI Analytics. FDA recall D-0080-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0080-2018. Source: US FDA. Licensed CC0.

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