Recall Register

Food recall: American Pure Whey, Whey Protein Matrix Chocolate flavor, 2 lb. and 5 lb. containers, Manufactured by American Pure…

Class I FDA enforcement event 72371. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

Undeclared Allergens; Soy and Milk.

Class I, in the words of FDA

a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death

American Pure Whey started this food recall on 6 Oct 2015. The firm address in the FDA record is in New Bern, NC. FDA put the recall in Class I. FDA event 72371 has 6 product records. The first FDA enforcement report date is 4 Nov 2015. The record gives the status Terminated, with the termination date 24 Jan 2017.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

AE, AZ, CA, CO, CT, DC, FL, IL, IN, KY, KS, MA, MD, MI, MO, NC, NE, NV, NY, OH, OK, OR, PA, TN, UT, VT, WA, WI and WY.

Recalling firm

American Pure Whey, New Bern, NC.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

6 product records in the event.

FDA event 72371: product records
Recall numberProductQuantityClassStatusReport date
F-0117-2016American Pure Whey, Whey Protein Matrix Chocolate flavor, 2 lb. and 5 lb. containers, Manufactured by American Pure Whey, Vanceboro, NC.350 units totalClass ITerminated4 Nov 2015
F-0118-2016American Pure Whey, Whey Protein Isolate (Chocolate flavor), 2 lb. and 5 lb. containers, Manufactured by American Pure Whey, Vanceboro, NC.N/AClass ITerminated4 Nov 2015
F-0119-2016Body Construct, Meal Replacement, Cinnamon Roll flavor, 2lb, Distributed by Body Construct.N/AClass ITerminated4 Nov 2015
F-0120-2016Build Your Own Body, Protein Powder, Manufactured for Build Your Own Body, Flagstaff Arizona.N/AClass ITerminated4 Nov 2015
F-0121-2016American Pure Whey, Whey Protein Matrix Vanilla flavor, 2 lb. and 5 lb. containers, Manufactured by American Pure Whey, Vanceboro, NC.N/AClass ITerminated4 Nov 2015
F-0122-2016American Pure Whey, Whey Protein Isolate (Vanilla flavor), 2 lb. and 5 lb. containers, Manufactured by American Pure Whey, Vanceboro, NC.N/AClass ITerminated4 Nov 2015

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class I: The highest of the three FDA recall classes.

The event in context

Food events that started in 2015
607
Share of these events in Class I
47%
Product records in this event
6
Events of the firm on the register
1

Official channels

Cite this page

Recall Register. FDA enforcement event 72371. https://recallregister.com/fda/i/72371/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA food enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: AE, AZ, CA, CO, CT, DC, FL, IL, IN, KY, KS, MA, MD, MI, MO, NC, NE, NV, NY, OH, OK, OR, PA, TN, UT, VT, WA, WI and WY.
What quantity of product is in FDA event 72371?
The event has 6 product records. The first record gives this quantity: 350 units total
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many food recalls of 2015 have the same class?
47% of the 607 food events that started in 2015 are in Class I.