03-21-2026, 05:00 PM
Nearly 90,000 bottles of children's ibuprofen recalled due to reports of foreign substances
By Mary Cunningham
March 20, 2026 / 2:54 PM EDT / CBS News
Nearly 90,000 bottles of children's ibuprofen are being recalled because they may contain a foreign substance, according to a notice issued by the U.S. Food and Drug Administration.
The recall affects Children's Ibuprofen Oral Suspension, a pain reliever that comes in liquid form. The product was manufactured in India by Strides Pharma for Taro Pharmaceuticals.
The medication is intended for children ages 2 to 11 and helps reduce pain and fever, according to a description of the product on Taro's website. The liquid ibuprofen comes in a berry flavor.
Strides Pharma initiated the recall on March 2 after receiving complaints that the bottles contained "a gel-like mass and black particles." The medication was distributed nationwide, the FDA said in its notice.
The FDA classified this as a Class II recall, which is when exposure to a product can create "temporary or medically reversible adverse health consequences," according to the agency's website.
The recall number for the product is D-0390-2026.
By Mary Cunningham
March 20, 2026 / 2:54 PM EDT / CBS News
Nearly 90,000 bottles of children's ibuprofen are being recalled because they may contain a foreign substance, according to a notice issued by the U.S. Food and Drug Administration.
The recall affects Children's Ibuprofen Oral Suspension, a pain reliever that comes in liquid form. The product was manufactured in India by Strides Pharma for Taro Pharmaceuticals.
The medication is intended for children ages 2 to 11 and helps reduce pain and fever, according to a description of the product on Taro's website. The liquid ibuprofen comes in a berry flavor.
Strides Pharma initiated the recall on March 2 after receiving complaints that the bottles contained "a gel-like mass and black particles." The medication was distributed nationwide, the FDA said in its notice.
The FDA classified this as a Class II recall, which is when exposure to a product can create "temporary or medically reversible adverse health consequences," according to the agency's website.
The recall number for the product is D-0390-2026.