US Drug Recall Register
Class II · Moderate risk Terminated Initiated Dec 18, 2019 (7 years ago)

Magic Bullet Supplement

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

Why it was recalled

Labeling: Incorrect or missing lot and/or expiration date. Products were compounded using expired components.

What was recalled

Magic Bullet Supplement

Recalling firm
MPRX, Inc. dba Medical Park Pharmacy
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0809-2020

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.