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Class IIITerminated in FDA datasetRecall initiated Jul 18, 2018

GU Energy Gels: Vanilla Bean, Gel; GUGEL 1 Pkt; item # 123017

Recalling firm: Advanced Food Concepts

Why it was recalled

Firm was notified by L-Leucine supplier that product may contain cyclamates. Testing of the product confirmed this and a recall was initiated.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Nov 14, 2019.

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Compare the exact product and package details with the label you have.

ProductGU Energy Gels: Vanilla Bean, Gel; GUGEL 1 Pkt; item # 123017, UPC: 769493100023; GUGEL 8Pkt Box, item # 123032, UPC: 769493900012; GUGEL 15 Serve Pkt, item # 124099, UPC: 769493100870; GUGEL 24Pkt Box; item number 123049, UPC:. 769493200020.
UPC769493100023, 769493100870, 769493900012

FDA code information

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Full FDA record and distribution details

Original product description

GU Energy Gels: Vanilla Bean, Gel; GUGEL 1 Pkt; item # 123017, UPC: 769493100023; GUGEL 8Pkt Box, item # 123032, UPC: 769493900012; GUGEL 15 Serve Pkt, item # 124099, UPC: 769493100870; GUGEL 24Pkt Box; item number 123049, UPC:. 769493200020.

Extracted codes and context

TypeCode / valueContext
UPC769493100023GU Energy Gels: Vanilla Bean, Gel; GUGEL 1 Pkt; item # 123017, UPC: 769493100023; GUGEL 8Pkt Box, item # 123032, UPC: 769493900012; GUGEL 15 Serve Pkt, item # 124099, UPC: 769493100870; GUGEL 24Pk
UPC769493100870ox, item # 123032, UPC: 769493900012; GUGEL 15 Serve Pkt, item # 124099, UPC: 769493100870; GUGEL 24Pkt Box; item number 123049, UPC:. 769493200020.
UPC769493900012 1 Pkt; item # 123017, UPC: 769493100023; GUGEL 8Pkt Box, item # 123032, UPC: 769493900012; GUGEL 15 Serve Pkt, item # 124099, UPC: 769493100870; GUGEL 24Pkt Box; item number 123049, UPC:. 769493200020.

Original FDA recall reason

Firm was notified by L-Leucine supplier that product may contain cyclamates. Testing of the product confirmed this and a recall was initiated.

Recall details

Recall number
F-1699-2018
Event ID
80591
FDA status
Terminated
Initiated
Jul 18, 2018
Reported
Aug 8, 2018
Classified
Jul 31, 2018
Terminated
Nov 14, 2019
Quantity
22, 848, 401 (All Domestically)
Location
Berkeley, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

worldwide distribution

FDA source record · F-1699-2018

Data updated September 16, 2026. View official FDA data ↗

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