AMPI Buttermilk Powder Recall: Metal Foreign Material Hazard
AMPI recalls Buttermilk Powder (formula 219) due to potential metal foreign material. Consumers should check product codes 7200.1.21.007.JF.01-007.JF.08 for affected items.
Lower-risk recall
The Buttermik powder may contain a Foreign Material (metal).
Contact the company
What happened, in plain English
AMPI is recalling Buttermilk Powder formula 219 because it may contain metal foreign material. This could pose a choking or injury risk if ingested. Affected products were distributed by Associated Milk Producers, Inc. in New Ulm, Minnesota. Read more at govinfonow.com/recall/14754-ampi-buttermilk-powder-recall-metal-foreign-material-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/14754-ampi-buttermilk-powder-recall-metal-foreign-material-hazard · Updated October 4, 2026 · FDA enforcement record: FDA #F-0376-2021
Cite this page
“AMPI Buttermilk Powder Recall: Metal Foreign Material Hazard.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14754-ampi-buttermilk-powder-recall-metal-foreign-material-hazard. Based on FDA recall #F-0376-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0376-2021%22&limit=1).
Why it’s dangerous
The buttermilk powder may contain metal fragments that could cause injury if ingested. This is a foreign material hazard that poses a choking risk, especially for young children.
Who’s affected
Consumers who purchased AMPI Buttermilk Powder formula 219 between the specified dates. Those with metal allergies or children under 5 are at slightly higher risk due to choking hazards.
How to tell if you have this one
Check for product codes 7200.1.21.007.JF.01 through 7200.1.21.007.JF.08 on the packaging. The product is sold in 25 kg (55.12 lbs) Kraft Paper Poly-lined bags.
- Brand
AMPI- Category
Food
What to do — step by step
Check Product Code
Look for the product code on the packaging to confirm if it's affected.
Where it went and when
Where it was distributed
Distributed in Wisconsin.
FDA distribution: “WI” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Wisconsin.
Recall timeline
FDA terminated this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0376-2021 (March 19, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0376-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.