CLASS II ONGOING Drug recall · Reported 27 Nov 2024 · FDA Enforcement Report

Vitamin B1, 100 mcg in blister card-foils unit dose recalled

Safecor Health is recalling Vitamin B1, 100 mcg in blister card-foils unit dose, www.safecorhealth.com, distributed nationwide in the US. The recall was initiated on 11 Nov 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot# 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 recalled3139 boxes

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0057-2025
FDA event ID
95659
Recalling firm
Safecor Health, Woburn, MA
Classification
Class II
Status
Ongoing
Recall initiated
11 Nov 2024
FDA classified
19 Nov 2024
Reported
27 Nov 2024
Type
Voluntary: Firm initiated
Customers notified by
Letter

Timeline

11 Nov 2024Recall initiated by company
19 Nov 2024Classified by FDA+8 days
27 Nov 2024Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity.

Product as listed by the FDA

Vitamin B1, 100 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-108-01

Where it was distributed

USA nationwide.

Nationwide

Questions about this recall

Is Vitamin B1, 100 mcg in blister card-foils unit dose, www.safecorhealth.com recalled?

Yes. Safecor Health recalled Vitamin B1, 100 mcg in blister card-foils unit dose, www.safecorhealth.com on 11 Nov 2024. The recall is Class II and its status is Ongoing. Recall number D-0057-2025.

Why was it recalled?

cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity.

Which lots are affected?

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

Where was it sold?

USA nationwide.

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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