Absonutrix Lyfetrition Vitamin B12 Bottles Missing Vitamin B12 - Recall
Absonutrix recalls Lyfetrition Vitamin B12 bottles that do not contain the listed vitamin B12. Consumers should check product labels for missing vitamin B12.
Lower-risk recall
The firm was informed that the product did not contain vitamin B12 (Methylcobalamyn) as listed on the label.
Contact the company
What happened, in plain English
Absonutrix is recalling Lyfetrition Vitamin B12 bottles because they do not contain the vitamin B12 listed on the label. This means the product may not provide the intended nutritional benefit. Read more at govinfonow.com/recall/19037-absonutrix-lyfetrition-vitamin-b12-bottles-missing-vitamin-b12-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/19037-absonutrix-lyfetrition-vitamin-b12-bottles-missing-vitamin-b12-recall · Updated October 7, 2026 · FDA enforcement record: FDA #F-1592-2018
Cite this page
“Absonutrix Lyfetrition Vitamin B12 Bottles Missing Vitamin B12 - Recall.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19037-absonutrix-lyfetrition-vitamin-b12-bottles-missing-vitamin-b12-recall. Based on FDA recall #F-1592-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1592-2018%22&limit=1).
Why it’s dangerous
The product does not contain vitamin B12 (Methylcobalamyn) as stated on the label. This means the supplement may not provide the intended nutritional benefit. The hazard is a failure to deliver the listed nutrient.
Who’s affected
People who bought Lyfetrition Vitamin B12 bottles from Absonutrix. Those who need vitamin B12 supplements are most at risk of not getting the intended nutrients.
How to tell if you have this one
Check for the product name 'Lyfetrition Live Life Nutritiously Vitamin B12 2 FL. OZ bottle' with UPC 7 00443 88822 6. Products were sold with specific lot numbers and expiration dates.
- Brand
Absonutrix- Product
Lyfetrition Live Life Nutritiously Vitamin B12 2 FL. OZ bottle Supplement Facts Serving Size:***Vitamin B-12 (as- Category
Food
What to do — step by step
Check Product Label
Look for the product name and UPC code to confirm if it's recalled.
Where it went and when
Where it was distributed
Distributed in 22 states.
FDA distribution: “Product was shipped to the following states: AL, CA, FL, GA, IL, IN, KY, MD, MA, MO, MT, NV, NJ, NY, NC, OH, OK, PA, TN, TX, UT & VA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, California, Florida, Georgia, Illinois, Indiana, Kentucky, Maryland, Massachusetts, Missouri, Montana, Nevada, New Jersey, New York, North Carolina, Ohio, Oklahoma, Pennsylvania, Tennessee, Texas, Utah, Virginia.
Recall timeline
FDA published this recall 23 days after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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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-1592-2018 (June 11, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1592-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.