F-0170-2020 Class II Terminated
FDA food recall F-0170-2020 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). Affected quantity: 262 bottles.
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 Quantity
- 262 bottles
Product Description
BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F
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
1820705, 1806004, 1733404, 1815204, 1719204, W0002670, W0000304, W000325, W0003878
Source
- Dataset
- openFDA food recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for F-0170-2020
- openFDA file date
- Nov 3, 2026
- Loaded by RegDataLab
- Nov 8, 2026