Bluebonnet Nutrition recalls EarthSweet Chewables CellularActive Methylfolate 1000 mcg due to label error showing 1000 mg instead of 1000 mcg. Consumers should check packaging for amber glass bottles with purple lids and expiration dates.
Label error during reprint. Says 1000 mg instead of 1000 mcg on the center front panel of the label.
Bluebonnet Nutrition is recalling EarthSweet Chewables Methylfolate 1000 mcg tablets because the label incorrectly states 1000 mg instead of 1000 mcg. This error could lead to an incorrect dosage if taken as a supplement.
The label error shows 1000 mg instead of 1000 mcg on the front panel. This could mean consumers take a much higher dose than intended, potentially causing adverse effects from excessive folic acid intake.
People who purchased EarthSweet Chewables CellularActive Methylfolate 1000 mcg tablets from Bluebonnet Nutrition. Those taking folic acid supplements are most at risk of incorrect dosing.
Check for amber glass bottles with purple lids and expiration dates of 8/2025 or 11/2025. The product has two different batch numbers: 30609501 and 30900501.
Look for the label error showing 1000 mg instead of 1000 mcg on the center front panel.
The label error shows 1000 mg instead of 1000 mcg on the front panel, which could lead to incorrect dosage if taken as a supplement.
Check for amber glass bottles with purple lids and expiration dates of 8/2025 or 11/2025. The product has two batch numbers: 30609501 and 30900501.
The recall does not specify a remedy, so consumers should check the label for the error and contact Bluebonnet Nutrition for further instructions.
We’ve drafted a message you can send Bluebonnet Nutrition to request your refund or repair — edit it as you like.
Subject: Recall F-1097-2024 — Bluebonnet Nutrition Bluebonnet Nutrition Hello, I own a Bluebonnet Nutrition that is covered by recall F-1097-2024 from Bluebonnet Nutrition. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
