FDA Food recall F-0179-2020
AquaLyte, 30g pkg./foil pouch, SKU: 1023
- FDA Food
- Class II
- terminated
- Published 2019-11-27
On 2019-11-27 the FDA classified a Class II recall of AquaLyte, 30g pkg./foil pouch, SKU: 1023 by Basic Reset, citing products do not conform to Dietary Supplement CGMP regulations.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-0179-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-09-23 |
| Published | 2019-11-27 |
| Last updated | 2026-09-13 11:50 UTC |
| Company | Basic Reset |
| Distribution | US |
Product
AquaLyte, 30g pkg./foil pouch, SKU: 1023
Reason
Products do not conform to Dietary Supplement CGMP regulations.
Identifiers
| code_info | 91117 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:50 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0179-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.