Recall archive / FDA food enforcement
Multiple Vitamin B Capsules, 60 Capsules, Biologically Active Forms of Vitamin B12, Folate, B6. Packaged in bottles u... — FDA record F-0841-2023
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Apr 20, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- 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
- undeclared allergen (milk)
- Classification
- Class I
- Recalling firm
- Euro-Pharma
- Quantity
- 23,770 units total
- Agency-reported status
- Terminated
- Source record identifier
- F-0841-2023
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | 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. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Nationwide
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Report date
- May 17, 2023
- Recall initiation date
- Apr 20, 2023
- Center classification date
- May 10, 2023
- Termination date
- Sep 19, 2023
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.