Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Dicloxacillin Sodium Capsules Recalled by Sandoz, Inc Due to Failed Impurities/Degradation Specifications:Out of specification result for a...

Date: May 2, 2016
Company: Sandoz, Inc
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Sandoz, Inc directly.

Affected Products

Dicloxacillin Sodium Capsules, USP 250mg, Rx Only, 100 Capsule Bottle, Manufactured in Austria by Sandoz Gmbh, Distributed by Sandoz Inc., Princeton, NJ 08540, Product of Spain, NDC 0781-2248-01

Quantity: 78,606 bottles

Why Was This Recalled?

Failed Impurities/Degradation Specifications:Out of specification result for a known impurity obtained during testing.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Sandoz, Inc

Sandoz, Inc has 12 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report