US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 3, 2018 (8 years ago)

Temozolomide 20 mg NDC 43975-0253-05 28 days supply

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Processing Controls.

What was recalled

Temozolomide 20 mg NDC 43975-0253-05 28 days supply

Recalling firm
Kroger Specialty Pharmacy, Inc.
NDC code
43975-0253-05
Origin
MS, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0780-2018

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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