FDAClass IIRecall started February 17, 2025

Ergocalciferol – Vitamin D Supplement – 10 mcg per 0.05 mL Oral Syringe Recall

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…

What is the FDA recall status?

The FDA record lists this recall as ongoing. FDA enforcement data is not a live recall-lifecycle tracker. Follow the official instructions and check the agency notice or firm for current guidance.

How FDA enforcement data reports status

Why was Ergocalciferol – Vitamin D Supplement – 10 mcg per recalled?

Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes.

What should I do if I have this product?

Follow the firm and FDA instructions for the affected product. Contact the recalling firm for current guidance.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare your product with the product description and available lot, UPC or model codes below from the official FDA record to check whether it is covered by this recall. If an identifier is missing or unclear, check the complete official notice or contact the firm; an incomplete match here does not establish that your product is unaffected.

Full product description

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.

Which lot codes, UPCs or models are affected?

Lot #: 24300812, Exp 01/31/2025; 24530836, Exp 07/19/2025

Agency record number
D-0250-2025
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…
Recalling firm
Safecor Health, LLC
Quantity
3069 Oral Syringes
Distribution
Nationwide in the USA
Recall started
February 17, 2025
Report date
March 12, 2025
Classification
Class II
Status
Ongoing
Agency
FDA (drug)
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