# FDA recall D-1153-2016

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

## Product

Atropine Sulfate Injection Solution, 0.4 mg/1 mL (0.4 mg/mL),  in a) 1 mL syringes and b) 2 mL syringes, Rx Only, Cantrell Drug Co., Little Rock, AR --- NDC 52533-010-45, UPC: 0100352533010453

## Reason for recall

Subpotent Drug

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1153-2016
- **Recalling firm:** Cantrell Drug Company
- **Classification:** Class I
- **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-1153-2016

## Citation

> AI Analytics. FDA recall D-1153-2016. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-1153-2016. Source: US FDA. Licensed CC0.

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