Safecor Vitamin B-1 Tablets Recall: Incorrect Ingredient Labeling
Safecor Health recalls vitamin B-1 tablets with incorrect thiamine labeling. This may cause ineffective treatment. Check product details to determine if affected.
Lower-risk recall
Box labeled Thiamine Hydrochloride instead of Thiamine Mononitrate
Contact the company
What happened, in plain English
Safecor Health is recalling vitamin B-1 tablets that are labeled with thiamine hydrochloride instead of thiamine mononitrate. This could lead to ineffective treatment since the two forms have different medical uses. Read more at govinfonow.com/recall/23212-safecor-vitamin-b-1-tablets-recall-incorrect-ingredient-labeling.
Source Summary by GovInfoNow · govinfonow.com/recall/23212-safecor-vitamin-b-1-tablets-recall-incorrect-ingredient-labeling · Updated October 9, 2026 · FDA enforcement record: FDA #F-0606-2017
Cite this page
“Safecor Vitamin B-1 Tablets Recall: Incorrect Ingredient Labeling.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23212-safecor-vitamin-b-1-tablets-recall-incorrect-ingredient-labeling. Based on FDA recall #F-0606-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0606-2017%22&limit=1).
Why it’s dangerous
Thiamine hydrochloride and thiamine mononitrate are different chemical forms. The recalled tablets contain the wrong form, which may not work as intended for medical treatments. This could lead to ineffective treatment if the product is used without proper medical guidance.
Who’s affected
People who have purchased Safecor Vitamin B-1 (THIAMINE) 100 mg tablets with NDC 48433-0108-01. Those taking the vitamin for medical reasons may be at higher risk if the incorrect ingredient is used.
How to tell if you have this one
Check for the product name 'Safecor Vitamin B-1 (THIAMINE) 100 mg tablets' with NDC code 48433-0108-01. The lot numbers A15012, A15021, 16A004, 16A015, and 16A035 are also affected.
- Brand
Safecor Health- Category
Food
What to do — step by step
Check Product Label
Look for the NDC code 48433-0108-01 and lot numbers A15012, A15021, 16A004, 16A015, or 16A035 on the packaging.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 11 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Do I need to stop using these tablets?
The recall does not require stopping use; check the product details to see if it's affected.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0606-2017 (September 12, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0606-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.