Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Levonorgestrel Recalled by Spectrum Laboratory Products, Inc. Due to CGMP Deviations: these repackaged and redistributed products are...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Spectrum Laboratory Products, Inc. directly.
Affected Products
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.
Quantity: 1 container
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Spectrum Laboratory Products, Inc.
Spectrum Laboratory Products, Inc. has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report