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SUN PHARMACEUTICAL INDUSTRIES INC recalls Niacin Extended-Release Tablets, USP 1000mg, Rx Only, 90 Tablets per bottle, Distributed by: Sun Pharmaceutical Industri

Recalled January 31, 2024 · FDA recall D-0269-2024 · SUN PHARMACEUTICAL INDUSTRIES

Hazard
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment. · FDA Class II
Units
6552 bottles
Sold at
Nationwide in the USA

Description

CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.

Product
Niacin Extended-Release Tablets, USP 1000mg, Rx Only, 90 Tablets per bottle, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Limited, Survey No. 259/15, Dadra-396 191(U.T. of D & NH), INDIA, NDC 47335-613-81.
Manufacturer(s)
SUN PHARMACEUTICAL INDUSTRIES INC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

SUN PHARMACEUTICAL INDUSTRIES INC recalls Niacin Extended-Release Tablets, USP 1000mg, Rx Only, 90 Tablets per bottle, Distributed by: Sun Pharmaceutical Industri | RecallWatchUSA