Food Recall Check
Class I · High risk Terminated Initiated Apr 20, 2023 (3 years ago)

Multiple Vitamin B Capsules recall

Recalled by Euro-Pharma · Green Bay, WI, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

undeclared allergen (milk)

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

Multiple Vitamin B Capsules, 60 Capsules, Biologically Active Forms of Vitamin B12, Folate, B6. Packaged in bottles under the following brands: 1. EuroMedica Active B Complex, Product #68006, UPC 3 67703 68006 0. Manufactured by a cGMP compliant facility exclusively for: Euromedica, 925 Challenger Drive, Green Bay, WI 54311. 2. Terry Naturally BioActive Vitamin B, Product #18006, UPC 3 67703-18006 5. Manufactured by a cGMP compliant facility exclusively for: EuroPharma, Inc., Green Bay, WI 54311.

Quantity: 23,770 units total

Food: Dietary supplements

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.

1. Active B, Lot # 1220019, Best By Date: November 2022; Lot # 0921232, Best By Date: July 2023; Lot # 0222190, Best By Date: January 2024. 2. BioActiva, Lot # 1220022, Best By Date: October 2022; Lot # 0921231, Best By Date: July 2023; Lot # 0222192, Best By Date: January 2024; Lot # 0223570, Best By Date: December 2024.

Where it was sold

Nationwide.

FDA's distribution note: Nationwide

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
Euro-Pharma
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 20, 2023
In FDA report of
May 17, 2023
Terminated
Sep 19, 2023
FDA recall number
F-0841-2023 · event 92162
Official record
FDA enforcement report search

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