# FDA recall D-0186-2017

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

## Product

Calcium Chloride (20 mg/mL) in 0.9% Sodium Chloride 500 mL Bag, Rx Only, Single-Dose Bag Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207,  NDC 52533-102-09

## Reason for recall

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

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0186-2017
- **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-0186-2017

## Citation

> AI Analytics. FDA recall D-0186-2017. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0186-2017. Source: US FDA. Licensed CC0.

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