Nature's Wonderland Sinus & Lung Care
Reason There was a mix-up with ingredients used. The product is an herbal blend consisting of 7 different herbs. The blend calls for Ginger Root; however, Ginkgo Leaves was accidentally added.
Nature's Wonderland brand Thyroid Formula 60 Veg Capsules recall
Recalled by Penn Herb Company, Ltd. · Philadelphia, PA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Potential Salmonella contamination
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Nature's Wonderland brand Thyroid Formula 60 Veg Capsules UPC: 715486893205. Packaged in White PET 150cc bottle with security closure
Quantity: 51 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 #:Sm32x Batch Lot #:23289A
Where it was sold
California Florida Illinois Maryland Michigan Missouri New York Ohio Pennsylvania
FDA's distribution note: Distributed to customers in PA, CA, IL, FL, MI, MD, MO, OH, and NY.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
- Penn Herb Company, Ltd.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 3, 2024
- In FDA report of
- Jul 10, 2024
- Terminated
- Feb 19, 2025
- FDA recall number
- F-1432-2024 · event 94762
- Official record
- FDA enforcement report search
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