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FDA News Release

Sonar Products ordered to cease operations, Stratus Pharmaceuticals ordered to cease distributing unapproved drugs

Companies distributed unapproved and adulterated drugs

For Immediate Release

June 15, 2017

Release

Today, U.S. District Judge Kathleen M. Williams for the Southern District of Florida entered a consent decree of permanent injunction between the United States and Stratus Pharmaceuticals Inc. of Miami, Florida, Sonar Products Inc. of Carlstadt, New Jersey and two of the companies’ officers, Alberto Hoyo and Juan Carlos Billoch.

According to the complaint filed with the consent decree, Stratus and Sonar routinely shipped unapproved, improperly labeled (misbranded), and substandard or contaminated (adulterated) drugs in interstate commerce. Specifically, Sonar manufactured and Stratus distributed a number of dermatological products, including various washes, creams and ointments that were not approved by the U.S. Food and Drug Administration, in violation of the Federal Food, Drug, and Cosmetic Act.

“These companies have endangered the public by selling products that have not been proven to be safe or effective and are poorly made,” said Janet Woodcock, M.D., director of the FDA’s Center for Drug Evaluation and Research. “The agency will continue to take aggressive enforcement action against those who repeatedly violate the law and put consumers at risk.”

In April 2015, U.S. Marshalls seized unapproved prescription drug products manufactured by Sonar and marketed and distributed by Stratus valued at more than $16 million. The unapproved products included:

  • a solution marketed to treat excessive sweating;
  • an antibiotic cleanser marketed for treatment of skin conditions, such as acne, rosacea and seborrhea;
  • a topical ointment marketed to treat wounds;
  • a topical cream and gel marketed to treat psoriasis, eczema and other skin conditions; and
  • drops used to treat ear pain.

Additionally, FDA inspections since 2014 found that Stratus and Sonar violated current good manufacturing practice (CGMP) requirements. The inspectors found Stratus failed to properly handle more than 1,300 consumer complaints. Among other significant CGMP violations, Sonar manufactured and released adulterated drugs, used components that did not meet established standards or specifications, failed to properly clean manufacturing equipment and used test methods that lacked a scientific basis.

The consent decree requires Sonar to cease operations until, among other things, it hires a CGMP expert, corrects its violations and receives written permission from the FDA to resume operations. Stratus is further prohibited from distributing unapproved drugs until it obtains required FDA approvals for those products.

The complaint was filed by the U.S. Department of Justice on behalf of the FDA.

The FDA, an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines and other biological products for human use, and medical devices. The agency also is responsible for the safety and security of our nation’s food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.
 

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Page Last Updated: 06/15/2017
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