Vitamin D3 Dietary Supplement Recalled for Packaging Defect
Safecor Health is recalling specific lots of Vitamin D3 25 mcg tablets due to a manufacturing defect where blister card-foils may separate from the blister cavity. No illnesses or injuries have been reported.
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: This is an FDA Class II recall without reported hospitalizations or illnesses. The hazard is a manufacturing defect affecting blister packaging integrity rather than contamination or direct product safety, and the source explicitly states no illnesses or injuries have been reported, making it a precautionary recall with theoretical risk only.
Plain-English summary
Safecor Health, LLC is recalling eight lots of Vitamin D3 25 mcg tablets. The recall was initiated due to manufacturing deviations where observations were made of blister card-foils separating from the blister cavity. The affected products are 100-count unit dose boxes distributed nationwide. The recalled lots and expiration dates are: Lot# 24A0052 (05/01/2026), 24A0057 (05/13/2026), 24A0066 (05/31/2026), 24A0067 (06/04/2026), 24A0068 (06/17/2026), 24A0069 (06/19/2026), 24A0075 (07/08/2026), and 24A0078 (07/12/2026). The product NDC is 48433-104-01.
No illnesses or injuries have been reported in connection with this recall. The manufacturing defect may affect the integrity of the tablets in the blister packaging.
The recalled product
- Product
- Vitamin D3, 25 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-104-01
- Manufacturer
- Safecor Health, LLC
- Category
- Drug — Dietary Supplement
- Affected units
- 7,488
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 (14)
- Lot# 24A0052
- exp. date 05/01/2026
- 24A0057
- exp. date 05/13/2026
- 24A0066
- exp. date 05/31/2026
- 24A0067
- exp. date 06/04/2026
- 24A0068
- exp. date 06/17/2026
- 24A0069
- exp. date 06/19/2026 24A0075
- exp. date 07/08/2026 24A0078
- exp. date 07/12/2026
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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