drugs Class II Updated 2013-01-30

West-ward Pharmaceutical Corp. recalls Lisinopril and Hydrochlorothiazide Tablets, 20 mg/25 mg, pac

Recalled Product

Lisinopril and Hydrochlorothiazide Tablets, 20 mg/25 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1264-01) and b) 1000-count tablets per bottle (NDC 0143-1264-10), Rx only, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724.

Hazard / Issue

Presence of Foreign Substance: Reports of gray smudges identified as minute stainless steel particulates were found in the recalled tablets.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot #: 69392A, 69393A, 69394A, 69395A, 69396A, 69397A , Exp 09/15; 69495A, 69496A, 69497A, 69498A, 69524A, 69525A, Exp 10/15
View official government recall

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