# FDA recall D-0882-2017

> **Spectrum Laboratory Products, Inc.** · Class II · drug recall initiated 2017-04-13.

## Product

Levonorgestrel, U.S.P. active pharmaceutical ingredient, packaged in 1 kg container, Rx only, Spectrum Chemical Mfg. Corp, Gardena, CA  90248, New Brunswick, NJ  08901, Product code L1229.

## Reason for recall

CGMP Deviations: these repackaged and redistributed products are being recalled due to a recall notice from the active pharmaceutical ingredient manufacturer for deviations from current Good Manufacturing Practices that were found during a recent FDA inspection.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0882-2017
- **Recalling firm:** Spectrum Laboratory Products, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-04-13
- **Report date:** 2017-06-14
- **Termination date:** 2019-02-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** New Brunswick, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0882-2017

## Citation

> AI Analytics. FDA recall D-0882-2017. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-0882-2017. Source: US FDA. Licensed CC0.

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