The drug was supplied to three different parties with three different brand names.
According to a notification issued by United States Food and Drug Administration, the recalling has been initiated voluntarily by the city-based drug maker and the same was intimated to the drug regulator through a letter on August 2.
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When contacted, a Dr Reddy's spokesperson said it is difficult to quantify number of bottles to be called and the financial impact in negligible.
Ranitidine Hydrochloride is indicated in gastro- oesophageal reflux disease, treatment of peptic ulcers, treatment of benign gastric ulceration, Zollinger-Ellison syndrome and treatment of duodenal ulceration.
According to FDA, the reason for recall was mentioned as "Microbial Contamination of Non-Sterile Products: A lot of raw material used in the manufacture of Ranitidine was positive for Pseudomonas sp."
While Equate brand (Acid Reducer) was distributed by Wal-Mart Stores Inc, Equaline brand and Wal-Zan brands were distributed by Supervalu Inc and Walgreen Co, the FDA notification said.
The recall has been initiated under Class II, which has been defined as 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.
DRL shares today settled higher by 3.19% at Rs 2,110.40 on the BSE.
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