Lupin recalls
Lupin appears in 4 official U.S. recall notices indexed by RecallRadar, most recently on 2017-11-29.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 4 |
|---|---|
| Published | 2016-09-14 to 2017-11-29 |
| By agency | FDA Drug (4) |
| By classification | Class III (3), Class II (1) |
| By status | terminated (4) |
| Distribution named in notices | US |
Recalls
- Pravastatin Sodium USP, tablets, 40 mg, 90-count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202,…
FDA Drug · Class II · 2017-11-29 · Lupin
Reason: 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. - Escitalopram Tablets USP 20 mg, 100-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Baltimore, MD, 21202, Manufactured by:…
FDA Drug · Class III · 2016-09-28 · Lupin
Reason: Labeling: Incorrect or Missing Lot and/or Expiration Date - Amlodipine Besylate Tablets USP, 2.5mg, 90-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc
FDA Drug · Class III · 2016-09-14 · Lupin
Reason: CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications. - Amlodipine Besylate Tablets USP, 10mg, 1000-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc
FDA Drug · Class III · 2016-09-14 · Lupin
Reason: CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.