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Class IIOngoing

Vitamin B1, 100 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorh… recall

FDA recall D-0057-2025 · initiated Nov 11, 2024

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Nov 27, 2024How we research

Safecor Health, LLC recalled Vitamin B1, 100 mcg, 1 tablet in blister card-foils, 100-count unit dose box, ww… in Nov 2024 — an FDA Class II recall (D-0057-2025) 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.

Lot# 24A0050, exp. date 04/25/2026; 24A0055, exp. date 05/09/2026; 24A0059, exp. date 05/16/2026; 24A0060, exp. date 05/20/2026; 24A0071, exp. date 06/24/2026; 24A0072, exp. date 06/26/2026

Quantity recalled: 3139 boxes

Details

Product
Vitamin B1, 100 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-108-01
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
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was Vitamin B1, 100 mcg, 1 tablet in blister card-foils, 100-count unit dose box, ww… recalled?
Safecor Health, LLC recalled Vitamin B1, 100 mcg, 1 tablet in blister card-foils, 100-count unit dose box, ww… in Nov 2024 — an FDA Class II recall (D-0057-2025) 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 B1, 100 mcg, 1 tablet in blister card-foils, 100-count unit dose box, ww… recalled?
Per the FDA enforcement record, the reason for recall D-0057-2025 was: cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity.
Is a recalled Vitamin B1, 100 mcg, 1 tablet in blister card-foils, 100-count unit dose box, ww… 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 B1, 100 mcg, 1 tablet in blister card-foils, 100-count unit dose box, ww… are affected?
Distributed: USA nationwide.. The recall covers these lots — Lot# 24A0050, exp. date 04/25/2026; 24A0055, exp. date 05/09/2026; 24A0059, exp. date 05/16/2026; 24A0060, exp. date 05/20/2026; 24A0071, exp. date 06/24/2026; 24A0072, exp. date 06/26/2026. 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-0057-2025.

Source: openFDA Drug Enforcement record D-0057-2025

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