Severity
Critical
CriticalClass ITerminated
FDA Food recall · Reported May 17, 2023
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 Ba
undeclared allergen (milk)
Euro-Pharma recalled Multiple Vitamin B Capsules, 60 Capsules, Biologically Active Forms of Vitamin B12, Folat… - a critical-severity action.
Multiple Vitamin B Capsules, 60 Capsules, Biologically Active Forms of Vitamin B12, Folat… was recalled by Euro-Pharma in May 17, 2023. Reason: undeclared allergen (milk). Check the official notice for the remedy. Verify recall #F-0841-2023 with the FDA Food before acting.
The recall
Euro-Pharma issued this critical-severity FDA Food recall-undeclared allergen (milk).
- Critical
- severity level
- 24K units
- affected scope
- Class I
- classification
- May 17, 2023
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0841-2023 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0841-2023) was formally reported on May 17, 2023, with the manufacturer initiating the action on April 20, 2023. It is classified under Critical severity (Class I), with a current status of Terminated. Euro-Pharma is listed as the recalling firm, operating out of Green Bay, WI. Federal records list the affected scope as 23,770 units total.
The documented reason for this recall is: undeclared allergen (milk) Distribution data in the federal record shows the product reached: Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
23,770 units total
Related Recalls
6
6 from same agency
Product description
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.
Reason for recall
undeclared allergen (milk)
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-0841-2023 |
| Date reported | May 17, 2023 |
| Date initiated | April 20, 2023 |
| Recalling firm | Euro-Pharma |
| Firm location | Green Bay, WI |
| Affected scope | 23,770 units total |
| Distribution | Nationwide |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0841-2023) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product 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.. Recalled by Euro-Pharma. Units affected: 23,770 units total.
Why was this product recalled? ▼
undeclared allergen (milk)
Which agency issued this recall? ▼
This recall was issued by the FDA Food on May 17, 2023. Severity: Critical. Recall number: F-0841-2023.
Where was the recalled product distributed? ▼
Distribution: Nationwide.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0841-2023) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported May 17, 2023. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.