BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle recalled over manufacturing violations
- Recall date
- September 23, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Basic Reset Inc. recalls BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F
- Recall number
- F-0170-2020
- FDA classification
- Class II
- Brand / firm
- Basic Reset Inc.
- Sold / distributed
- 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.
Why it was recalled
Products do not conform to Dietary Supplement CGMP regulations.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F
Get recall alerts
Free email alert whenever Basic Reset Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Basic Reset Inc.