Lupin, Sun Pharma recall drugs in US market

Lupin and Sun Pharma are recalling different products in the US, according to the US Food and Drug Administration (USFDA).

Lupin is recalling 11,688 bottles of Lisinopril tablets USP, 10 mg, which is used to treat high blood pressure, in the US market, as per the latest Enforcement Report by the US health regulator.

USFDA said the company is recalling the specific number of bottles due to presence of foreign tablets.

Lisinopril tablets USP, (20 mg) were found in a 1,000 count bottle of Lisinopril Tablets USP (10 mg), it noted.

The tablets have been manufactured at Lupin’s Nagpur facility and the nationwide (US) recall has been initiated by its Baltimore-based arm — Lupin Pharmaceuticals, on July 17.

The USFDA has classified it as a Class-II recall, which 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”.

When contacted, a company spokesperson said the recall is limited to the US market and does not impact any other markets.

Similarly, a US-based subsidiary of Sun Pharma is recalling 3,516 bottles of antiepileptic drug, Clonazepam orally disintegrating tablets.

The USFDA listed the reason for the recall as “cross-contamination with other products”.

The Sun Pharmaceutical Industries initiated the nationwide recall on July 6.

The USFDA has classified the action as a Class-III recall, which is initiated in a situation “in which use of or exposure to a violative product is not likely to cause adverse health consequences.”