Bluebonnet Methylfolate Chewables Recalled for Label Unit Error
Bluebonnet Nutrition is recalling EarthSweet Chewables CellularActive Methylfolate 1000 mcg due to a labeling error stating '1000 mg' instead of '1000 mcg' on the front label.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: FDA Class III recall for a minor labeling error. The product was manufactured correctly at 1000 mcg, but the front label incorrectly states 1000 mg instead of 1000 mcg. No illnesses or injuries reported. Labeling errors on Class III recalls typically score 2 per the rubric.
Plain-English summary
Bluebonnet Nutrition Corporation is recalling EarthSweet Chewables CellularActive Methylfolate 1000 mcg (90-tablet bottles in amber glass with purple lid) due to a label printing error.
The center front panel of the label incorrectly states the dose as "1000 mg" instead of the correct "1000 mcg." The product itself was manufactured correctly at 1000 mcg, but the labeling error could cause confusion about the actual potency of the supplement.
The recall affects 3,365 bottles distributed to retail stores for sale. Affected batches have expiration dates of August 2025 or November 2025, with specific manufacturing and packaging lot numbers noted in the FDA recall notice.
Consumers who have purchased this product should check their bottle's labeling against the lot numbers in the FDA recall notice. If you have an affected bottle, consult your healthcare provider about whether to continue use or dispose of the product.
The recalled product
- Product
- EarthSweet¿ Chewables CellularActive¿ Methylfolate 1000 mcg; 90 chewable tablets packaged in an amber glass botte with purple lid
- Manufacturer
- Bluebonnet Nutrition Corporation (Dairy Ashford)
- Hazard
- labeling-error
- unit-mislabeling
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- Expiration 8/2025 & Expiration 11/2025 Item 0455
- Label Code F
- Manufacturing Batch Record # 306095- Packaging Lot # 30609501 Item 0455
- Manufacturing Batch Record # 309005- Packaging Lot # 30900501
Distribution
Distribution scope not specified by the agency.
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