F-0175-2020 Class II Terminated

Recalled by Basic Reset Inc. — Hendersonville, TN

FDA food recall F-0175-2020 was initiated by Basic Reset Inc. on Sep 23, 2019 and is designated Class II. Reason for recall: Products do not conform to Dietary Supplement CGMP regulations. The recall status is terminated (terminated Aug 19, 2020).

Recall Details

Product Type
Food
Report Date
Nov 27, 2019
Initiation Date
Sep 23, 2019
Termination Date
Aug 19, 2020
Voluntary/Mandated
FDA Mandated

Product Description

Ionyte 4 fl. oz. plastic bottle, SKU: 100-1B

Reason for Recall

Products do not conform to Dietary Supplement CGMP regulations.

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.

Code Information

29049,28343,27618A,19018B, 35317B,101617,08518A, 29123

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for F-0175-2020
openFDA file date
Nov 3, 2026
Loaded by RegDataLab
Nov 8, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for F-0175-2020. Report a data issue: hello@regdatalab.com.