Buttermilk Powder, Formula 219

Ampi recalled Buttermilk Powder, Formula 219 in an FDA Class II enforcement action reported as F-0376-2021. The Buttermik powder may contain a Foreign Material (metal).

Metal fragments can cause cuts, choking or internal injury. Do not inspect or taste a suspect product.

Children, older adults and anyone who may swallow a fragment without noticing are at greater risk.

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop eating or using the product; do not try to find the fragment by tasting or chewing. Seek medical care if anyone has swallowed metal or has severe throat, chest or abdominal pain. Keep the packaging and contact the retailer or manufacturer about a refund.

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-0376-2021 and keep the packaging, lot code and proof of purchase if you have them.

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

This page is normalized from the openFDA enforcement record F-0376-2021. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.