FDA Recall United States TerminatedTerminated: November 14, 2019Historical recordClass III
Advanced Food Concepts
- Product
- GU Energy Stroopwafels; Dutch-Style syrup filled waffle coo…
- Published
- August 8, 2018
- Distribution
- worldwide distribution
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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass III
Firm was notified by L-Leucine supplier that product may contain cyclamates. Testing of the product confirmed this and a recall was initiated.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| GU Energy Stroopwafels; Dutch-Style syrup filled waffle cookie; Campfire Smores, Waffle; WAFFLE 1 Pkt, Item # 124380, UPC: 769493102683; WAFFLE 16 Pkt Box, Item # 124379, UPC: 769493102676; | 769493102683 | 22, 848, 401 (All Domestically) | All lots |
This recall shares FDA event ID 80591 with 10 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: November 14, 2019Historical recordClass III
FDA Recall United States TerminatedTerminated: November 14, 2019Historical recordClass III
FDA Recall United States TerminatedTerminated: November 14, 2019Historical recordClass III
FDA Recall United States TerminatedTerminated: November 14, 2019Historical recordClass III
FDA Recall United States TerminatedTerminated: November 14, 2019Historical recordClass III
FDA Recall United States TerminatedTerminated: November 14, 2019Historical recordClass III
FDA Recall United States TerminatedTerminated: November 14, 2019Historical recordClass III
FDA Recall United States TerminatedTerminated: November 14, 2019Historical recordClass III
FDA Recall United States TerminatedTerminated: November 14, 2019Historical recordClass III
FDA Recall United States TerminatedTerminated: November 14, 2019Historical recordClass III
Responsible company: Advanced Food Concepts
FDA Recall United States TerminatedTerminated: November 14, 2019Historical recordClass III
FDA Recall United States TerminatedTerminated: November 14, 2019Historical recordClass III
FDA Recall United States TerminatedTerminated: November 14, 2019Historical recordClass III
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