Magic Bullet Supplement
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-D-0809-2020.
Labeling: Incorrect or missing lot and/or expiration date. Products were compounded using expired components.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-D-0809-2020.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Mprx, Inc. Dba Medical Park Pharmacy or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-D-0809-2020.
MPRX, Inc. dba Medical Park Pharmacy
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Mprx, Inc. Dba Medical Park Pharmacy Recall FAQ
Mprx, Inc. Dba Medical Park Pharmacy is the subject of a supplements safety report: Magic Bullet Supplement. The notice was published on December 18, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 1 units are potentially affected.