FDA recall D-0882-2017

Spectrum Laboratory Products, Inc. · Class II · drug

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

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

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