# FDA recall D-1159-2016

> **Cantrell Drug Company** · Class II · drug recall initiated 2015-08-21.

## Product

HEParin Sodium 0.5 USP UNITS/mL in 0.225% SODIUM CHLORIDE, in 3 mL Syringe, Rx Only, Cantrell Drug Co., Little Rock, AR --- UPC: 9999992212

## Reason for recall

Stability Data Does Not Support Expiry

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1159-2016
- **Recalling firm:** Cantrell Drug Company
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-08-21
- **Report date:** 2016-07-13
- **Termination date:** 2017-02-03

- **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-1159-2016

## Citation

> AI Analytics. FDA recall D-1159-2016. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-1159-2016. Source: US FDA. Licensed CC0.

---

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