CLASS III Food recall · Reported 14 Dec 2016 · FDA Enforcement Report

Safecor Vitamin B-1 (Thiamine) recalled by Safecor Health

Safecor Health is recalling Safecor Vitamin B-1 (Thiamine), distributed nationwide in the US. The recall was initiated on 12 Sep 2016 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesSafecor Health Lot # A15012, A15021, 16A004, 16A015 and 16A035
Quantity recalled1431 boxes

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0606-2017
FDA event ID
75196
Recalling firm
Safecor Health, Woburn, MA
Brand
Safecor
Classification
Class III
Status
Terminated
Recall initiated
12 Sep 2016
FDA classified
6 Dec 2016
Reported
14 Dec 2016
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons
Product category
Vitamins

Timeline

12 Sep 2016Recall initiated by company
6 Dec 2016Classified by FDA+85 days
14 Dec 2016Published 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

Box labeled Thiamine Hydrochloride instead of Thiamine Mononitrate

Product as listed by the FDA

Safecor Vitamin B-1 (THIAMINE) 100 mg tablets NDC: 48433-0108-01 Distributed by: SAFECOR HEALTH, 317 NEW BOSTON STREET, WOBURN, MA

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Box labeled Thiamine Hydrochloride instead of Thiamine Mononitrate

Which lots are affected?

Safecor Health Lot # A15012, A15021, 16A004, 16A015 and 16A035

Where was it sold?

Nationwide

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 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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