Lupin recalls
FDA enforcement reports naming Lupin Limited as the recalling firm.
- Recall reports
- 3
- Class I (serious)
- 0
- Most recent report
- Nov 29, 2017
- Nov 29, 2017Pravastatin Sodium USP, tablets, 40 mg, 90-count bottle, Rx only, Manufactured for: Lup…Drug · Lupin LimitedPresence of foreign tablets/capsules: This product lot is being recalled due to a pharmacy complaint where one Duloxetine Delayed Release Capsule, 30mg was found in a Pravastatin Sodium Tablets USP, 40mg bottle.Class II
- Sep 14, 2016Amlodipine Besylate Tablets USP, 2Drug · Lupin LimitedCGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.Class III
- Sep 14, 2016Amlodipine Besylate Tablets USP, 10mg, 1000-count bottles, Rx only, Manufactured for: L…Drug · Lupin LimitedCGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.Class III