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Sun Pharmaceutical Industries, Inc.

Sun Pharmaceutical Industries, Inc. Recalls

All product recalls associated with Sun Pharmaceutical Industries, Inc..

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Recall Summary

Total Recalls

125

Past Year

Class I (Serious)

Most Recent

Oct 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 121–125 of 125 recalls

Carvediol 6.25mg Tablets (Sun Pharma) – Failed Impurities Test (2016)

Failed Impurities/Degradation Specifications

Class IIILow

FDAJun 27, 2016Nationwide• Sun Pharmaceutical Industries, Inc.

Carvediol 25mg Tablets (Sun Pharma) – Failed Impurities Test (2016)

Failed Impurities/Degradation Specifications

Class IIILow

FDAJun 27, 2016Nationwide• Sun Pharmaceutical Industries, Inc.

Carvediol 3.125mg Tablets (Sun Pharma) – Failed Impurities Test (2016)

Failed Impurities/Degradation Specifications

Class III

1...5 67

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Low

FDAJun 27, 2016Nationwide• Sun Pharmaceutical Industries, Inc.

Carvediol 12.5mg Tablets (Sun Pharma) – Failed Impurities Test (2016)

Failed Impurities/Degradation Specifications

Class IIILow

FDAJun 27, 2016Nationwide• Sun Pharmaceutical Industries, Inc.

Nimodipine Capsules (Sun Pharma) – crystallization risk (2013)

Crystallization; crystallized nimodipine

Class IIModerate

FDAMay 21, 2013Nationwide• Sun Pharmaceutical Industries Inc.