<p> New Delhi: Dr Reddy's Laboratories is recalling over 8,000 bottles of a generic medication used to prevent rejection of a transplanted organ from the US market due to a packaging error, according to the US Food & Drug Administration.</p>.<p> The Hyderabad-based drug major is recalling 8,280 bottles of Tacrolimus capsules from the US market for 'presence of foreign tablets/capsules' in the affected lot.</p>.<p> One 0.5 mg Tacrolimus capsule was found in a bottle of 1 mg Tacrolimus capsules, the USFDA stated in its latest Enforcement Report.</p>.Centre orders new drug-making standards after overseas deaths.<p> The affected lot was produced at Dr Reddy's Bachupally-based plant near Hyderabad.</p>.<p> New Jersey-based Dr Reddy's Laboratories, Inc has initiated the nationwide (US) Class II recall on December 15, 2023.</p>.<p> As per the USFDA, a Class II recall is initiated in a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.</p>.<p> Dr Reddy's had recalled 4,000 bottles of the same drug in March last year as well. The company had initiated the recall on February 8, 2023. </p>
<p> New Delhi: Dr Reddy's Laboratories is recalling over 8,000 bottles of a generic medication used to prevent rejection of a transplanted organ from the US market due to a packaging error, according to the US Food & Drug Administration.</p>.<p> The Hyderabad-based drug major is recalling 8,280 bottles of Tacrolimus capsules from the US market for 'presence of foreign tablets/capsules' in the affected lot.</p>.<p> One 0.5 mg Tacrolimus capsule was found in a bottle of 1 mg Tacrolimus capsules, the USFDA stated in its latest Enforcement Report.</p>.Centre orders new drug-making standards after overseas deaths.<p> The affected lot was produced at Dr Reddy's Bachupally-based plant near Hyderabad.</p>.<p> New Jersey-based Dr Reddy's Laboratories, Inc has initiated the nationwide (US) Class II recall on December 15, 2023.</p>.<p> As per the USFDA, a Class II recall is initiated in a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.</p>.<p> Dr Reddy's had recalled 4,000 bottles of the same drug in March last year as well. The company had initiated the recall on February 8, 2023. </p>