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Actavis Laboratories, FL, Inc.

Actavis Laboratories, FL, Inc. Recalls

All product recalls associated with Actavis Laboratories, FL, Inc..

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Feb 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.

Showing 21–25 of 25 recalls

Diclofenac Sodium Tablets (Actavis) – Tablet Split Risk (2014)

Failed Tablet/Capsule Specifications: Recall due to complaints of split or broken tablets.

Class IIModerate

FDAApr 24, 2014Nationwide• Actavis Laboratories, FL, Inc.

Trelstar Injectable Suspension (Actavis) – Labeling Error (2013)

Labeling: Label Error On Declared Strength: Trelstar 11.25 mg labeled carton/kit contained a vial labeled as 3.75 mg instead of a vial being labeled as 11.25mg.

Class IIModerate

FDADec 9, 2013Nationwide• Actavis Inc