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

Lupron Depot 22.5 mg 3 month Kit NDC 00074-3346-03 84 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

Lupron Depot 22.5 mg 3 month Kit NDC 00074-3346-03 84 days supply

Recalling firm
Kroger Specialty Pharmacy, Inc.
NDC code
00074-3346-03
Origin
MS, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0800-2018

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.