Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to CGMP Deviations: product was manufactured that did not...

Date: July 16, 2019
Company: Deva Holding AS - Cerkezkoy Subesi
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 Deva Holding AS - Cerkezkoy Subesi directly.

Affected Products

Temozolomide Capsules, 140 mg, packaged in a) 5-count bottle (NDC 67877-540-07), b) 14-count bottle (NDC 67877-540-14), Rx only, Manufactured by: Deva Holding A.S., 1 Merkez Mahallesi, Istanbul, Turkey 34303, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054.

Quantity: a) 7380 bottles; b) 10332 bottles

Why Was This Recalled?

CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Deva Holding AS - Cerkezkoy Subesi

Deva Holding AS - Cerkezkoy Subesi has 6 total recalls tracked by RecallDetector.

Related Recalls

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