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.
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: 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
- Hazard
- blister-separation
- manufacturing-defect
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.
Related recalls
Same category
- CriticalWarfarin Tablets Recalled After Mix-Up Between 2.5 mg and 5 mg Strengths
FDA (Drugs) · 2026-07-21
- ModerateFDA Recalls Pred Mild Ophthalmic Suspension Due to Failed Stability Specifications
FDA (Drugs) · 2026-06-03
- ModerateNicotine Transdermal System Patches Recalled for Oxidative Impurity Specification Failure
FDA (Drugs) · 2026-06-03
- ModerateGas-X Simethicone 125 mg softgels recall for incomplete labeling
FDA (Drugs) · 2026-05-27
- HighLiraglutide Injection Recalled Due to Particulate Matter in Cartridges
FDA (Drugs) · 2026-05-27