FDA Recall United States TerminatedTerminated: March 22, 2022Historical recordClass II
NSE Products, Inc.
- Product
- Pharmanex Kids Jungamals, Dietary Supplement 90 Chewable Tab…
- Published
- November 10, 2021
- Distribution
- Nationwide
NSE Products, Inc. Recall: Nu Skin announces a voluntary field action for Pharmanex ageLOC TR90 Protein Boost due to an undeclared milk allergen. - F-1532-2017
United States
TerminatedClass I
- Company
- NSE Products, Inc.
- Product
- Pharmanex ageLOC TR90 Protein Boost. Protein Powder. Net wt.…
- Recall date
- January 26, 2017
- Terminated
- July 5, 2017
- Source
- FDA
Reason for recall
Nu Skin announces a voluntary field action for Pharmanex ageLOC TR90 Protein Boost due to an undeclared milk allergen.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Pharmanex ageLOC TR90 Protein Boost. Protein Powder. Net wt. 1.59 lbs (720g). 30 Servings. Natural Vanilla Flavor. Lactose, Gluten, & Soy Free. Plant Protein/Vegetarian. | Not published in this source record | 21,460 units | Lot Numbers: AZ30751, AZ32051, AZ00661, AZ27161, and AZ34161 |
Distribution
- Nationwide and Canada. No other foreign or VA/govt/military consignees.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1532-2017
- Event ID
- 76341
- Status
- Terminated
- Classification
- Class I
- Company
- NSE Products, Inc.
- Product description
- Pharmanex ageLOC TR90 Protein Boost. Protein Powder. Net wt. 1.59 lbs (720g). 30 Servings. Natural Vanilla Flavor. Lactose, Gluten, & Soy Free. Plant Protein/Vegetarian.
- Quantity
- 21,460 units
- Reason
- Nu Skin announces a voluntary field action for Pharmanex ageLOC TR90 Protein Boost due to an undeclared milk allergen.
- Recall initiation date
- January 26, 2017
- Report date
- March 15, 2017
- Classification date
- Not published in this source record
- Termination date
- July 5, 2017
- Distribution pattern
- Nationwide and Canada. No other foreign or VA/govt/military consignees.
- UPC, lot, and code information
- Lot Numbers: AZ30751, AZ32051, AZ00661, AZ27161, and AZ34161
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Press Release
- 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.
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Virginia | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
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 I mean?
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of July 5, 2017.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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.