AMPI Buttermilk Powder, formula 219. 25 KG Net (55.12 Lbs Net). Distributed by: Associated Milk Producers, Inc., New Ulm, Minnesota 5...
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0376-2021.
The Buttermik powder may contain a Foreign Material (metal).
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0376-2021.
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 Ampi 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-F-0376-2021.
AMPI
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.
Ampi Recall FAQ
Ampi is the subject of a dairy safety report: AMPI Buttermilk Powder, formula 219. 25 KG Net (55.12 Lbs Net). Distributed by: Associated Milk Producers, Inc., New Ulm, Minnesota 5.... The notice was published on March 19, 2021 by the U.S. Food and Drug Administration (FDA). Approximately 621 units are potentially affected.