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Micro Labs Usa, Inc S Recalls
6 recalls on record · November 5, 2014 to March 18, 2015 · Drugs
Recalls by year
14
15
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
March 18, 2015DrugsFDA
Micro Labs Usa, Inc S recalls Simvastatin Tablets, USP, 80mg, Rx Only, 90 count bottles, Manufactured by: Micro Labs Limited Goa-403 722, India, Manuf
Hazard: Failed Impurities/Degradation Specifications: Product failed a known impurity specification.
March 18, 2015DrugsFDA
Micro Labs Usa, Inc S recalls Simvastatin Tablets, USP, 40mg, Rx Only, 90 count bottles, Manufactured by: Micro Labs Limited Goa-403 722, India, Manuf
Hazard: Failed Impurities/Degradation Specifications: Product failed a known impurity specification.
March 18, 2015DrugsFDA
Micro Labs Usa, Inc S recalls Simvastatin Tablets, USP, 20mg a) 90- count bottle (42517-0020-10), b) 1000-count-bottle (NDC 42571-0020-10), Rx only,
Hazard: Failed Impurities/Degradation Specifications: Product failed a known impurity specification.
November 26, 2014DrugsFDA
Micro Labs Usa, Inc S recalls LOSARTAN POTASSIUM TABLETS USP, 25 mg, 1000 Tablet Bottles, Rx Only. Manufactured by: Micro Labs Limited, Goa-403 722, I
Hazard: Failed Content Uniformity Specifications; Dry mix failed blend uniformity.
November 19, 2014DrugsFDA
Micro Labs Usa, Inc S recalls Simvastatin Tablets, USP, 10 mg, Rx Only, 90 count bottles, Manufactured by: Micro Labs Limited, Goa-403 722, INDIA, Man
Hazard: Failed Impurities/Degradation Specifications: Product failed Impurity content (Butylated Hydroxy Anisole Content) against shelf life specification.
November 5, 2014DrugsFDA
Micro Labs Usa, Inc S recalls GLIMEPIRIDE TABLETS, USP 2 mg, a)100 count bottle, (NDC 42571-101-01), b) 500 count Bottle (NDC 42571-101-05), Rx only,
Hazard: Failed Stability Specifications: Micro Labs is recalling two lots due to out of specification results during stability testing.