# FDA recall D-0088-2019

> **GLAXOSMITHKLINE NEBRASKA** · Class II · drug recall initiated 2018-09-26.

## Product

Prevacid 24HR (Lansoprazole) delayed-release capsules, 15 mg, 14 capsules per bottle in a carton containing 1 bottle (NDC: 0067-6286-14), 2 bottles (NDC: 0067-6286-28) or 3 bottles (NDC: 0067-6286-42), Over-the-counter, Distributed By: GSK Consumer Healthcare, Warren, NJ 07059.

## Reason for recall

CGMP deviations

## Distribution

Nationwide USA and Puerto Rico

## Key facts

- **Recall number:** D-0088-2019
- **Recalling firm:** GLAXOSMITHKLINE NEBRASKA
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-09-26
- **Report date:** 2018-10-17
- **Termination date:** 2020-11-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lincoln, NE, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0088-2019

## Citation

> AI Analytics. FDA recall D-0088-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0088-2019. Source: US FDA. Licensed CC0.

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