# FDA recall D-0195-2017

> **Cantrell Drug Company** · Class II · drug recall initiated 2016-11-18.

## Product

HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-006-04

## Reason for recall

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0195-2017
- **Recalling firm:** Cantrell Drug Company
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-11-18
- **Report date:** 2016-12-21
- **Termination date:** 2020-04-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Little Rock, AR, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0195-2017

## Citation

> AI Analytics. FDA recall D-0195-2017. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-0195-2017. Source: US FDA. Licensed CC0.

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