DrugNov 26, 2014
Micro Labs Usa, Inc S LOSARTAN POTASSIUM TABLETS USP, 25 mg, 1000 Tablet Bottles recall — FDA D-0253-2015
Failed Content Uniformity Specifications; Dry mix failed blend uniformity.
Class IIFDA: TerminatedMicro Labs Usa, Inc S
Recall history in this database
Classification mix: Class II: 2, Class III: 1.
DrugNov 19, 2014
Micro Labs Usa, Inc S Simvastatin Tablets, USP, 10 mg recall — FDA D-0246-2015
Failed Impurities/Degradation Specifications: Product failed Impurity content (Butylated Hydroxy Anisole Content) against shelf life specification.
Class IIIFDA: TerminatedMicro Labs Usa, Inc S
DrugNov 5, 2014
GLIMEPIRIDE TABLETS, USP 2 mg, a)100 count bottle, (NDC 42571-101-01), b) 500 count Bottle recall — FDA D-0046-2015
Failed Stability Specifications: Micro Labs is recalling two lots due to out of specification results during stability testing.
Class IIFDA: TerminatedMicro Labs Usa, Inc S
Understanding this recall history
This page summarizes recall records in which the official source identifies Micro Labs Usa, Inc S as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.