FDA Drugs recall ·
Ergocalciferol - Vitamin D Supplement - 10 mcg (400 Units) per 0.05 mL… recall
- Recall number
- D-0250-2025
- Date
- (initiated February 17, 2025)
- Company / brand
- Safecor Health, LLC
4060 Business Park Dr Ste B, Columbus, OH, United States - Category
- Drugs › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 3069 Oral Syringes
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Ergocalciferol - Vitamin D Supplement - 10 mcg (400 Units) per 0.05 mL Oral Syringe, Delivers: 0.05 mL Oral Solution, Mfg by: Westminster, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: 69367028302.
Why was it recalled?
Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot #: 24300812, Exp 01/31/2025; 24530836, Exp 07/19/2025
Distribution
Nationwide in the USA
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (drugs), recall D-0250-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.