PlainRecalls
FDA Drug Low Class III Terminated

Fluoxetine Capsules USP, 20 mg, 100 count bottle, Rx Only, 100 Capsules, Sandoz Inc Princeton, NJ 08540 NDC 0781-2822-01

Reported: December 17, 2014 Initiated: December 5, 2014 #D-0291-2015

Product Description

Fluoxetine Capsules USP, 20 mg, 100 count bottle, Rx Only, 100 Capsules, Sandoz Inc Princeton, NJ 08540 NDC 0781-2822-01

Reason for Recall

Labeling: Illegible Label: Sandoz Inc. is recalling of one lot of Fluoxetine Capsules due to an illegible logo on the capsule.

Details

Recalling Firm
Sandoz Incorporated
Units Affected
1,008 bottles
Distribution
AZ
Location
Broomfield, CO

Frequently Asked Questions

What product was recalled?
Fluoxetine Capsules USP, 20 mg, 100 count bottle, Rx Only, 100 Capsules, Sandoz Inc Princeton, NJ 08540 NDC 0781-2822-01. Recalled by Sandoz Incorporated. Units affected: 1,008 bottles.
Why was this product recalled?
Labeling: Illegible Label: Sandoz Inc. is recalling of one lot of Fluoxetine Capsules due to an illegible logo on the capsule.
Which agency issued this recall?
This recall was issued by the FDA Drug on December 17, 2014. Severity: Low. Recall number: D-0291-2015.