Recalls / Class II
Class IIF-0175-2020
Product
Ionyte 4 fl. oz. plastic bottle, SKU: 100-1B
- Type
- Food
- Affected lot / code info
- 29049,28343,27618A,19018B, 35317B,101617,08518A, 29123
- Quantity
- N/A
Why it was recalled
Products do not conform to Dietary Supplement CGMP regulations.
Recalling firm
- Firm
- Basic Reset Inc.
- Notification channel
- Type
- FDA Mandated
- Address
- 260 W Main St Ste 103, N/A, Hendersonville, Tennessee 37075-7316
Distribution
- Distribution pattern
- 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.
Timeline
- Recall initiated
- 2019-09-23
- FDA classified
- 2019-11-21
- Posted by FDA
- 2019-11-27
- Terminated
- 2020-08-19
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-0175-2020. The FDA issues recall classifications as health-hazard assessments, not legal findings.