Dr Reddy's to recall 1,752 bottles of heartburn drug in the US

The ongoing Class III recall is on account of "Discolouration" and
because the product contains brown pellets, USFDA said. As per the US
health regulator, a class III recall is initiated in a situation "in
which use of or exposure to a violative product is not likely to cause
adverse health consequences".

https://economictimes.indiatimes.com/industry/healthcare/biotech/pharmaceuticals/dr-reddys-to-recall-1752-bottles-of-heartburn-drug-in-the-us/articleshow/75656114.cms