Nature's Wonderland Sinus & Lung Care Recalled for Ingredient Mix-Up
Penn Herb Company is recalling Nature's Wonderland Sinus & Lung Care capsules because Ginkgo Leaves were accidentally added to the herbal blend instead of Ginger Root.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class III, which indicates the product is unlikely to cause adverse health consequences. The hazard involves an unintended ingredient substitution (Ginkgo Leaves instead of Ginger Root) without reported injuries or illnesses, fitting the criteria for a moderate severity labeling or formulation error.
Plain-English summary
Penn Herb Company, Ltd. is recalling 10 bottles of Nature's Wonderland Sinus & Lung Care, 60 VCaps (Capsules), PET bottle. The product is an herbal blend consisting of seven different herbs. The recall is due to an ingredient mix-up where Ginkgo Leaves were accidentally added to the blend, which calls for Ginger Root.
The affected product is identified by Lot# 16344A. The product was distributed throughout the United States.
Consumers should stop using the product and return it to the place of purchase for a refund or contact the recalling firm for further instructions.
The recalled product
- Product
- Nature's Wonderland Sinus & Lung Care, 60 VCaps (Capsules), PET bottle
- Manufacturer
- Penn Herb Company, Ltd.
- Category
- Food — Dietary Supplement
- Affected units
- 10
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot# 16344A
Distribution
Distribution scope not specified by the agency.
Related recalls
Same manufacturer · Penn Herb Company, Ltd.
See all →- SevereThyroid Supplement Recalled for Potential Salmonella Contamination
FDA (Food) · 2024-07-10
Same hazard · mis labeling
See all →- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02
- HighSura Tanmen Ramen Noodles Recalled for Undeclared Fish Allergens
FDA (Food) · 2026-09-02
- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-09-02