Recall · openFDA Food Enforcement
AquaLyte, 30g pkg./foil pouch, SKU: 1023: FDA Recall F-0179-2020 Agency action: Sep 23, 2019 Record ID: F-0179-2020
View official source ↗ What happened Original notice title
AquaLyte, 30g pkg./foil pouch, SKU: 1023, recall F-0179-2020
From the archived source record
Products do not conform to Dietary Supplement CGMP regulations.
What the official notice says to do Check the original notice for the instructions that apply to the named product, company, and affected lots.
Read the official notice → Status and source details
Status recorded in the archive Terminated
FDA recall classification Class II
Recall initiated by FDA Mandated
Report date Nov 27, 2019
Termination date in the archive Aug 19, 2020
Source checked Jul 16, 2026
Record revision 7a770e0a9704 This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.
Sources, dates, and coverage → What is affected Product AquaLyte, 30g pkg./foil pouch, SKU: 1023 Company Basic Reset Inc. Lot / identifier 91117 Market / distribution Product was shipped to all 50 states. Product was shipped to the following foreign consignees: Canada, Nigeria, U.K., Australia, Israel, Puerto Rico, Virgin Islands, Hungary, UAE, Mexico, Philippines, Greece, and Puerto Rico. Quantity reported N/A What is affected Product AquaLyte, 30g pkg./foil pouch, SKU: 1023 Company Basic Reset Inc. Lot / identifier 91117 Market / distribution Product was shipped to all 50 states. Product was shipped to the following foreign consignees: Canada, Nigeria, U.K., Australia, Israel, Puerto Rico, Virgin Islands, Hungary, UAE, Mexico, Philippines, Greece, and Puerto Rico. 