Vitamin D3, 25 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhe… recall
FDA recall D-0056-2025 · initiated Nov 11, 2024
Safecor Health, LLC recalled Vitamin D3, 25 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www… in Nov 2024 — an FDA Class II recall (D-0056-2025) because cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity.
May cause temporary or medically reversible harm; low probability of serious harm.
Why it was recalled
cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity.
Labelling, packaging or a product mix-up
The wrong information — or the wrong medicine — ended up in the pack. A mix-up is a manufacturing failure that can still be dangerous to swallow.
This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.
Is your product affected? Check the lot number
A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.
Quantity recalled: 7488 boxes
Details
- Product
- Vitamin D3, 25 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-104-01
- Recalling company
- Safecor Health, LLC
- Classification
- Class II
- Status
- Ongoing
- Type
- Voluntary: Firm initiated
- Distribution
- USA nationwide.
- Initiated
- Nov 11, 2024
- FDA report date
- Nov 27, 2024
Frequently asked
- Was Vitamin D3, 25 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www… recalled?
- Safecor Health, LLC recalled Vitamin D3, 25 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www… in Nov 2024 — an FDA Class II recall (D-0056-2025) because cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity. May cause temporary or medically reversible harm; low probability of serious harm.
- Why was Vitamin D3, 25 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www… recalled?
- Per the FDA enforcement record, the reason for recall D-0056-2025 was: cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity.
- Is a recalled Vitamin D3, 25 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www… dangerous to take?
- An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
- Which lots of Vitamin D3, 25 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www… are affected?
- Distributed: USA nationwide.. The recall covers these lots — 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. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0056-2025.