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Lupin Pharmaceuticals Inc.

Lupin Pharmaceuticals Inc. Recalls

All product recalls associated with Lupin Pharmaceuticals Inc..

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Recall Summary

Total Recalls

1000

Past Year

303

Class I (Serious)

Most Recent

Nov 2025

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.

Showing 2961–2980 of 4747 recalls

Ceftriaxone Injection 250mg (Lupin) – CGMP Deviation (2016)

CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.

Class IIILow

FDAMar 11, 2016Nationwide• Lupin Pharmaceuticals Inc.

Ceftriaxone Sodium (Lupin) – Ingredient Specification Failure (2016)

CGMP Deviations: active pharmaceutical ingredient intermediates failed specifications.

Class IIILow

FDAMar 11, 2016Nationwide• Lupin Pharmaceuticals Inc.

Amikacin Sulfate Injection (Teva) – Glass Particulate (2016)

Presence of Particulate Matter: particulate matter identified as glass in one vial.

Class I

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High

FDAMar 9, 2016Nationwide• Teva Pharmaceuticals USA

L'Bri Aloe Health Juice (Cosmetic Labs) – undeclared ingredient (2016)

Product contains ingredients that are not on the label including sodium metabisulfite, to which a part of the population may be sensitive.

Class IIILow

FDAMar 2, 2016Nationwide• Cosmetic Labs LP

Fluconazole Injection (Sagent) – Cross Contamination (2016)

Cross contamination with other products: metronidazole

Class IIModerate

FDAMar 1, 2016Nationwide• Sagent Pharmaceuticals Inc

Telmisartan Tablets 80mg (Torrent) – Foreign Substance (2016)

Presence of Foreign Substance: Product complaint for the presence of foreign matter identified as silicone within the tablet.

Class IIILow

FDAFeb 25, 2016Nationwide• Torrent Pharmaceuticals Limited

Paliperidone Tablets (Mylan) – Dissolution Specification Failure (2016)

Failed Dissolution Specifications; three month stability time point.

Class IIModerate

FDAFeb 12, 2016Nationwide• Mylan Pharmaceuticals Inc.

Morphine Sulfate Injection (Pharmakon) – Super-Potent Drug (2016)

Super-Potent Drug: Out of specification for potency results (high) were obtained for one lot of morphine sulfate Inj.

Class IHigh

FDAFeb 11, 2016IL, IN• Pharmakon Pharmaceuticals

Snowmobiles (Arctic Cat) – Crash and Injury Hazard (2016)

This recall involves all model year 2016 Arctic Cat turbo 9000 snowmobiles. Recalled models include the M 9000, XF 9000, XF9000 Cross Trek and ZR 9000 snowmobiles. The recalled snowmobiles were sold in the colors black, green, orange and white. The model name is on a decal on the top of the chassis between the seat and the rear bumper. The name Arctic Cat is on each side of the snowmobiles. The letter G in the 10th position of the vehicle identification number (VIN) indicates that the unit was made in the 2016 model year. The VIN is stamped into the chassis near the right foot rest.

CPSCFeb 10, 2016Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.

Prenatal Vitamin (DNE Nutraceuticals) – Folic acid potency (2016)

Adwe Prenatal tablets are being recalled due to a concern of potency of folic acid.

Class IIModerate

FDAFeb 8, 2016NY• DNE Nutraceuticals Inc.

Tudorza Pressair (AstraZeneca) – Defective Counter (2016)

Defective Delivery System: Some units have actuation counters set to a number other than 60.

Class IIModerate

FDAFeb 5, 2016Nationwide• AstraZeneca Pharmaceuticals LP

Paricalcitol Capsules (Teva) – Impurity Specification Failure (2016)

Failed Impurities/Degradation Specifications: Out of specification test results for impurities during stability testing.

Class IIModerate

FDAFeb 5, 2016Nationwide• Teva Pharmaceuticals USA

Menthocin Patch (Bonita) – Unapproved Marketing (2016)

Marketed without an approved NDA/ANDA

Class IIModerate

FDAJan 27, 2016Nationwide• Bonita Pharmaceuticals, LLC

Virt-Nate Prenatal (Virtus) – incorrect tablet imprint (2016)

Tablets/Capsules Imprinted with Wrong ID; product debossed with an incorrect punch. Bottles could contain tablets debossed with V259 (debossing for PreTab) instead of the correct punch, V264 (debossing for Virt-Nate).

Class IIILow

FDAJan 15, 2016MI• Virtus Pharmaceuticals, Llc

Risperidone Orally Disintegrating Tablets 2mg (Zydus) – impurity specs (2016)

Failed Impurities/Degradation Specifications: Out of specification for a known degradant.

Class IIILow

FDAJan 14, 2016Nationwide• Zydus Pharmaceuticals USA Inc

Daytrana 15mg Patch (Noven) – Delivery System Defect (2015)

Defective Delivery System: Out of Specification (OOS) results for the mechanical peel force (MPF) and z-statistic value which relates to the patients and caregiver ability to remove the release liner from the patch adhesive prior to administration.

Class IIModerate

FDADec 21, 2015Nationwide• Noven Pharmaceuticals, Inc.