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