# FDA recall D-911-2013

> **Braintree Laboratories Inc.** · Class III · drug recall initiated 2013-07-15.

## Product

Braintree HalfLytely and Bisacodyl Tablet Bowel Prep Kit (Rx)   NDC 52268-523-02

## Reason for recall

Defective Container; Small micro fracture observed in the 2-Liter bottle at the fill line resulting in a small leak when patient reconstitutes the bulk powder

## Distribution

Nationwie

## Key facts

- **Recall number:** D-911-2013
- **Recalling firm:** Braintree Laboratories Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-07-15
- **Report date:** 2013-08-28
- **Termination date:** 2014-01-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Holbrook, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-911-2013

## Citation

> AI Analytics. FDA recall D-911-2013. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/D-911-2013. Source: US FDA. Licensed CC0.

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