FDAClass IINovember 27, 2019

BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic recall: CGMP Deviations

BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F

Why was BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic 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?

1820705, 1806004, 1733404, 1815204, 1719204, W0002670, W0000304, W000325, W0003878

Product
BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F
Recalling firm
Basic Reset Inc.
Quantity
262 bottles
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)
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