FDA Recall United States Terminated Historical recordClass I
NSE Products, Inc.
- Product
- Pharmanex ageLOC TR90 Protein Boost. Protein Powder. Net wt.…
- Published
- March 15, 2017
- Distribution
- Nationwide
NSE Products, Inc. Recall: Pharmanex Jungamals was found to have a missing fish allergen statement on the label due to fish gelatin as a sub-component of the Vitamin E ingredient.
United States
TerminatedClass II
- Company
- NSE Products, Inc.
- Product
- Pharmanex Kids Jungamals, Dietary Supplement 90 Chewable Tab…
- Recall date
- October 1, 2021
- Terminated
- March 22, 2022
- Source
- FDA
Reason for recall
Pharmanex Jungamals was found to have a missing fish allergen statement on the label due to fish gelatin as a sub-component of the Vitamin E ingredient.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Pharmanex Kids Jungamals, Dietary Supplement 90 Chewable Tablets, white bottle, NSE Products Inc., Provo, UT 84601 1-888-PHARMANEX | Not published in this source record | 470 bottles | Batch Code: CS11711; Expiration Date: April 30, 2022 |
Distribution
- Distributed directly to consumers nationwide.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0095-2022
- Event ID
- 88804
- Status
- Terminated
- Classification
- Class II
- Company
- NSE Products, Inc.
- Product description
- Pharmanex Kids Jungamals, Dietary Supplement 90 Chewable Tablets, white bottle, NSE Products Inc., Provo, UT 84601 1-888-PHARMANEX
- Quantity
- 470 bottles
- Reason
- Pharmanex Jungamals was found to have a missing fish allergen statement on the label due to fish gelatin as a sub-component of the Vitamin E ingredient.
- Recall initiation date
- October 1, 2021
- Report date
- November 10, 2021
- Classification date
- Not published in this source record
- Termination date
- March 22, 2022
- Distribution pattern
- Distributed directly to consumers nationwide.
- UPC, lot, and code information
- Batch Code: CS11711; Expiration Date: April 30, 2022
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: NSE Products, Inc.
Other recalls from NSE Products, Inc.
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 II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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.
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