Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bottles and 200 count b
Summary
The FDA issued a Class II for Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bro by Blueroot Health, Inc.. Reason: Contains undeclared egg, soy, and hazelnut.
Details
Source
Food Recall
External ID
H-0663-2026
Action Date
2026-04-15
Status
Ongoing
Category
food
Product Description
Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bottles and 200 count bottles
Lot/Code Info: 100 count bottles - UPC: 693465524114,693465000083 Lot: 25E04-A, 25E04-B, 25E04 Expiration date: 05/27 200 count bottles - UPC:693465524213,693465000090 Lot: 25E04-B Expiration date: 05/27
Quantity Affected: 11,849 bottles
Reason for Recall
Contains undeclared egg, soy, and hazelnut
Distribution
Alaska, Arizona, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Maine, Michigan, Minnesota, Mississippi, Montana, North Carolina, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia, & Wyoming
Type: Voluntary: Firm initiated
Recall Initiated: 2026-03-27
Company
Middletown, CT
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 29 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Blueroot Health, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Blueroot Health, Inc. have FDA actions?
This is the only FDA action we have on record for Blueroot Health, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0663-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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