AquaLyte recall: CGMP Deviations
AquaLyte, 30g pkg./foil pouch, SKU: 1023
Why was AquaLyte recalled?
Products do not conform to Dietary Supplement CGMP regulations.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
91117
- Product
- AquaLyte, 30g pkg./foil pouch, SKU: 1023
- Recalling firm
- Basic Reset Inc.
- Quantity
- N/A
- 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.
- Recall date
- November 27, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (food)