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AMPI Recall: The Buttermik powder may contain a Foreign Material (metal).

United States

TerminatedClass II

Company
AMPI
Product
AMPI Buttermilk Powder, formula 219. 25 KG Net (55.12 Lbs N…
Recall date
March 19, 2021
Terminated
May 18, 2021
Source
FDA

Reason for recall

The Buttermik powder may contain a Foreign Material (metal).

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
AMPI Buttermilk Powder, formula 219. 25 KG Net (55.12 Lbs Net). Distributed by: Associated Milk Producers, Inc., New Ulm, Minnesota 56073. Packaged in Kraft Paper Poly-lined bags. Not published in this source record 621 - 25 kg bags 7200.1.21.007.JF.01 through 7200.1.21.007.JF.08

Distribution

  • WI

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0376-2021
Event ID
87582
Status
Terminated
Classification
Class II
Company
AMPI
Product description
AMPI Buttermilk Powder, formula 219. 25 KG Net (55.12 Lbs Net). Distributed by: Associated Milk Producers, Inc., New Ulm, Minnesota 56073. Packaged in Kraft Paper Poly-lined bags.
Quantity
621 - 25 kg bags
Reason
The Buttermik powder may contain a Foreign Material (metal).
Recall initiation date
March 19, 2021
Report date
April 7, 2021
Classification date
Not published in this source record
Termination date
May 18, 2021
Distribution pattern
WI
UPC, lot, and code information
7200.1.21.007.JF.01 through 7200.1.21.007.JF.08
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: AMPI

Other recalls from AMPI

FDA Recall United States Terminated Historical recordClass II

AMPI

Product
AMPI Whey Powder, Sweet Type, Formula 521, Extra Grade, spra…
Published
August 1, 2018
Distribution
Multiple states

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Wisconsin 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.