Pharmanex Kids Jungamals
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.
Pharmanex ageLOC TR90 Protein Boost recall
Recalled by NSE Products, Inc. · Provo, UT, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Nu Skin announces a voluntary field action for Pharmanex ageLOC TR90 Protein Boost due to an undeclared milk allergen.
Undeclared allergen: Milk
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
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
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot Numbers: AZ30751, AZ32051, AZ00661, AZ27161, and AZ34161
Where it was sold
Nationwide.
Virginia
FDA's distribution note: Nationwide and Canada. No other foreign or VA/govt/military consignees.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- NSE Products, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 26, 2017
- In FDA report of
- Mar 15, 2017
- Terminated
- Jul 5, 2017
- FDA recall number
- F-1532-2017 · event 76341
- Official record
- FDA enforcement report search