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All product recalls associated with Lupin Limited.
Total Recalls
5
Past Year
0
Class I (Serious)
1
Most Recent
Nov 2017
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Presence 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.
Contraceptive Tablets Out of Sequence- First 4 pills of the packet are brown, instead of the last four pills and the expiry/lot was not printed on the package.
Labeling: Incorrect or Missing Lot and/or Expiration Date
CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.