Sandoz Incorporated Recall: Fluoxetine Capsules USP, 20 mg, 100 count bottle, Rx Only, 100
Sandoz Incorporated Recall: Fluoxetine Capsules USP, 20 mg, 100 count bottle, Rx Only, 100 is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Sandoz Incorporated; Product: Fluoxetine Capsules USP, 20 mg, 100 count bottle, Rx Only, 100 Capsules, Sandoz Inc Princeton, NJ 08540 NDC 0781-2822
| Recalling firm | Sandoz Incorporated |
|---|---|
| Product | 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. |
| Classification | Class III (least serious — unlikely to cause adverse health consequences) |
| Status | Terminated |
| Distribution | AZ |
| Recall initiated | 20141205 |
| Recall number | D-0291-2015 |
| Category | drug |
| State | CO |
| Country | United States |
$29/mo
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