Methylfolate Chewables (Bluebonnet) – Label Error (2024)
Class III: A situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences
Class III recall indicates unlikely adverse health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
EarthSweet¿ Chewables CellularActive¿ Methylfolate 1000 mcg; 90 chewable tablets packaged in an amber glass botte with purple lid
Brand
Bluebonnet Nutrition Corporation (Dairy Ashford)
Lot Codes / Batch Numbers
Expiration 8/2025 & Expiration 11/2025 Item 0455, Label Code F, Manufacturing Batch Record # 306095- Packaging Lot # 30609501 Item 0455, Label Code F, Manufacturing Batch Record # 309005- Packaging Lot # 30900501
Products Sold
Expiration 8/2025 & Expiration 11/2025 Item 0455, Label Code F, Manufacturing Batch Record # 306095- Packaging Lot # 30609501 Item 0455, Label Code F, Manufacturing Batch Record # 309005- Packaging Lot # 30900501
Bluebonnet Nutrition Corporation (Dairy Ashford) is recalling EarthSweet¿ Chewables CellularActive¿ Methylfolate 1000 mcg; 90 chewable tablets packaged in an ambe due to Label error during reprint. Says 1000 mg instead of 1000 mcg on the center front panel of the label.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Label error during reprint. Says 1000 mg instead of 1000 mcg on the center front panel of the label.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 6, 2026