FDA Recall United States Terminated Historical recordClass I
Penn Herb Company, Ltd.
- Product
- Nature's Wonderland brand Thyroid Formula 60 Veg Capsules UP…
- Published
- July 10, 2024
- Distribution
- Distributed to customers in PA, CA, IL,…
Penn Herb Company, Ltd. Recall: 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.
United States
TerminatedClass III
- Company
- Penn Herb Company, Ltd.
- Product
- Nature's Wonderland Sinus & Lung Care, 60 VCaps (Capsules),…
- Recall date
- January 17, 2017
- Terminated
- April 27, 2018
- Source
- FDA
Reason for recall
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.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Nature's Wonderland Sinus & Lung Care, 60 VCaps (Capsules), PET bottle | Not published in this source record | 10 bottles | Lot# 16344A |
Distribution
- Product distributed throughout United States
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1528-2017
- Event ID
- 76423
- Status
- Terminated
- Classification
- Class III
- Company
- Penn Herb Company, Ltd.
- Product description
- Nature's Wonderland Sinus & Lung Care, 60 VCaps (Capsules), PET bottle
- Quantity
- 10 bottles
- 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.
- Recall initiation date
- January 17, 2017
- Report date
- March 1, 2017
- Classification date
- Not published in this source record
- Termination date
- April 27, 2018
- Distribution pattern
- Product distributed throughout United States
- UPC, lot, and code information
- Lot# 16344A
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Penn Herb Company, Ltd.
Other recalls from Penn Herb Company, Ltd.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class III mean?
A situation in which use of or exposure to a product is not likely to cause adverse health consequences.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
