Recall Radar

NSE Products recalls Pharmanex Kids Jungamals: allergen risk

November 10, 2021 · NSE Products Class II

Class IIFDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.
Reason for the recallPharmanex 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.

Find the official FDA enforcement report

Recall at a glance

Recalling company
NSE Products
Location
Provo, UT
Reported by FDA
November 10, 2021
Recall started
October 1, 2021
Risk class
Class II
Status (latest data we have)
Terminated
Type
Voluntary: Firm initiated
Category
Supplements and infant formula
Reason type
Undeclared allergensLabeling and quality

Is my product affected?

Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.

  • Pharmanex Kids Jungamals, Dietary Supplement 90 Chewable Tablets, white bottle, NSE Products Inc., Provo, UT 84601 1-888-PHARMANEX
    Quantity: 470 bottles
    Codes: Batch Code: CS11711; Expiration Date: April 30, 2022

Where it was distributed

Distributed directly to consumers nationwide.

What to do

If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.

Frequently asked questions

What was recalled?

NSE Products recalled 1 product, including Pharmanex Kids Jungamals, Dietary Supplement 90 Chewable Tablets, white bottle, NSE Products Inc., Provo, UT 84601 1-888-PHARMANEX.

Why was it recalled?

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.

What does Class II mean?

FDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.

Where was it sold or shipped?

Distributed directly to consumers nationwide.

What should I do if I have this product?

Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.

Similar recalls in supplements and infant formula

Sources

Data provided by the U.S. Food and Drug Administration (FDA) through openFDA, shown as published and not validated by this site. This site is independent and is not affiliated with or endorsed by FDA. It covers FDA-regulated foods; meat, poultry and egg products are regulated by USDA. Do not rely on this site for medical decisions: for health concerns contact a healthcare professional, and always follow the official notice and the company’s instructions. Terms and disclaimer.