Recall Register

Food recall: Amino Life brand Product - L-Leucine Instant Sunflower 25 Kgs Fiber carton double layer polyethylene bag as liner

Class III FDA enforcement event 80358. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

This recall has been identified due to the detection of cyclamates (artificial sweetener). Use of or consumption of cyclamates may include potential health hazard. Cyclamates and its salts (such as calcium cyclamate, sodium cyclamate, magnesium cyclamate, and potassium cyclamate) are currently prohibited from use in the United States.

Class III, in the words of FDA

a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences

Prinova US LLC started this food recall on 22 Jun 2018. The firm address in the FDA record is in Carol Stream, IL. FDA put the recall in Class III. FDA event 80358 has 4 product records. The first FDA enforcement report date is 1 Aug 2018. The record gives the status Terminated, with the termination date 15 May 2019.

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.

CA, IL, NV, PA, TN, TX, UT

Recalling firm

Prinova US LLC, Carol Stream, IL.

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

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

Products

4 product records in the event.

FDA event 80358: product records
Recall numberProductQuantityClassStatusReport date
F-1657-2018Amino Life brand Product - L-Leucine Instant Sunflower 25 Kgs Fiber carton double layer polyethylene bag as liner1775 kgsClass IIITerminated1 Aug 2018
F-1658-2018Amino Life brand Product - BCAA 2:1:1 Instant Sunflower 25 Kgs Fiber carton double layer polyethylene bag as liner1225 kgsClass IIITerminated1 Aug 2018
F-1659-2018Prinova brand Product - MRI Amintoten Strawberry Powder 25 Kgs Fiber carton double layer polyethylene bag as liner3350 kgsClass IIITerminated1 Aug 2018
F-1660-2018Prinova brand Product - Reginator NV (41825) 25 Kgs Fiber carton double layer polyethylene bag as liner3000 kgsClass IIITerminated1 Aug 2018

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 III: The lowest of the three FDA recall classes.

The event in context

Food events that started in 2018
578
Share of these events in Class III
10%
Product records in this event
4Median of the firm: 4
Events of the firm on the register
2

Other events of the firm

Other FDA enforcement events of Prinova US LLC
InitiatedProduct (first record)TypeClassRecords
16 Oct 2015Pea protein 85% dry powder in a 20 KG bag. Event 72600FoodClass I1

Official channels

Cite this page

Recall Register. FDA enforcement event 80358. https://recallregister.com/fda/iii/80358/. 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: CA, IL, NV, PA, TN, TX, UT
What quantity of product is in FDA event 80358?
The event has 4 product records. The first record gives this quantity: 1775 kgs
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many food recalls of 2018 have the same class?
10% of the 578 food events that started in 2018 are in Class III.