# FDA recall D-0321-2018

> **Intrathecal Compounding Specialist, LLC** · Class II · drug recall initiated 2017-11-30.

## Product

All sterile drug preparations remaining within expiry prepared from Hydromorphone Base Solution dispensed between October 16, 2017 and November 17, 2017, Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.

## Reason for recall

Lack of sterility assurance.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0321-2018
- **Recalling firm:** Intrathecal Compounding Specialist, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-11-30
- **Report date:** 2018-02-14
- **Termination date:** 2019-05-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Scott, LA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0321-2018

## Citation

> AI Analytics. FDA recall D-0321-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0321-2018. Source: US FDA. Licensed CC0.

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