# FDA recall D-1075-2017

> **Cantrell Drug Company** · Class II · drug recall initiated 2017-07-14.

## Product

Sodium Bicarbonate 8.4% Injection Solution 50 mL, 50 mEq (1mEq/mL) Single-Dose Syringe,  Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222

## Reason for recall

Lack of Sterility Assurance.

## Distribution

Nationwide within the US

## Key facts

- **Recall number:** D-1075-2017
- **Recalling firm:** Cantrell Drug Company
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-07-14
- **Report date:** 2017-08-16
- **Termination date:** 2020-09-16

- **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-1075-2017

## Citation

> AI Analytics. FDA recall D-1075-2017. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/D-1075-2017. Source: US FDA. Licensed CC0.

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