Byron White FORMULAS A-FNG Herbal Supplement
Reason Label does not declare walnuts in English
GNC Vitamin B-6 100mg 100 VEGETARIAN TABLETS DIETARY SUPPLEMENTS Distributed by recall
Recalled by General Nutrition Inc · Pittsburgh, PA, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
The firm was notified by a customer that the bottle contains green and white capsules instead of the usual white round tablets. They contacted their manufacturer to investigate the issue and the manufacture stated that there was a problem at the filling line. Bottles labeled as Vitamin B6 actually contained Pycnogenol.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
GNC Vitamin B-6 100mg 100 VEGETARIAN TABLETS DIETARY SUPPLEMENTS Distributed by: General Nutrition Corporation Pittsburgh, PA 15222 UPC 0 48107 20584 3
Quantity: 16,244/60 ct bottles
Food: Dietary supplements
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Item Code: 255219, Lot no.: 2990IV2552 Best By: 08/24
Where it was sold
FDA's distribution note: Product was shipped to all 50 US states and the following foreign countries: BOLIVIA, CHINA, GUAM, GUATEMALA, HONDURAS, KOREA MILITARY, MONGOLIA, PHILIPPINES, ROMANIA, SINGAPORE, SOUTH ARFICA & TURKS & CAICOS.
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- General Nutrition Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 27, 2022
- In FDA report of
- Sep 21, 2022
- Terminated
- Dec 23, 2022
- FDA recall number
- F-1734-2022 · event 90536
- Official record
- FDA enforcement report search
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