Vitamin B1 Supplement Recalled for Blister Packaging Defect
Safecor Health is recalling certain Vitamin B1 supplements due to manufacturing defects where blister card-foils are separating from the blister cavity.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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 II recall involving a manufacturing defect in product packaging. No illnesses or injuries have been reported. The defect affects packaging integrity but does not involve contamination or immediate safety hazard.
Plain-English summary
Safecor Health, LLC is recalling Vitamin B1, 100 mcg tablets due to a manufacturing defect. Observations revealed that some blister card-foils were separating from the blister cavity, which can affect the integrity of the product packaging.
The affected product was distributed nationwide in the United States. A total of 3,139 boxes were distributed. The recall involves lot numbers 24A0050 (expiration 04/25/2026), 24A0055 (expiration 05/09/2026), 24A0059 (expiration 05/16/2026), 24A0060 (expiration 05/20/2026), 24A0071 (expiration 06/24/2026), and 24A0072 (expiration 06/26/2026). The product is sold through www.safecorhealth.com with NDC 48433-108-01.
The recalled product
- Product
- Vitamin B1, 100 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-108-01
- Manufacturer
- Safecor Health, LLC
- Category
- Drug — Vitamin Supplement
- Affected units
- 3,139
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 (12)
- Lot# 24A0050
- exp. date 04/25/2026
- 24A0055
- exp. date 05/09/2026
- 24A0059
- exp. date 05/16/2026
- 24A0060
- exp. date 05/20/2026
- 24A0071
- exp. date 06/24/2026
- 24A0072
- exp. date 06/26/2026
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 5 recalled by Safecor Health, LLC under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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