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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Food
Food & Beverages/Dietary Supplements

Absonutrix: The firm was informed that the product did not contain vitamin B12 (Methylcobalamyn) as listed on the label.

Agency Publication Date: June 22, 2018
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Summary

Absonutrix has voluntarily recalled 78 bottles of Lyfetrition Live Life Nutritiously Vitamin B12 (2 FL. OZ). The recall was initiated because the product was found to contain no vitamin B12 (Methylcobalamyn) despite being labeled as a supplement. These products were distributed to 22 states including CA, NY, FL, and TX.

Risk

The product lacks the active ingredient Vitamin B12 listed on the supplement facts panel, which may result in a lack of expected nutritional benefits or health outcomes for consumers relying on this supplement.

What You Should Do

  1. Check your supplement bottles for the brand 'Lyfetrition Live Life Nutritiously Vitamin B12' in 2 FL. OZ sizes.
  2. Verify if your product matches UPC 7 00443 88822 6 and one of the affected lot numbers: 160318-2 (Exp: 03/2019) or ASM4192017 (Exp: 04-2020).
  3. If your product matches the recalled identifiers, contact Absonutrix at their Greensboro, NC location (5500 Adams Farm Lane, Suite 206) or via the FDA hotline for guidance.
  4. For further information or to report a complaint, call the FDA Consumer Complaint line at 1-888-723-3332 (1-888-SAFEFDA).

Affected Products

Product: Lyfetrition Live Life Nutritiously Vitamin B12 (2 FL. OZ)
UPC Codes:
700443888226
Lot Numbers:
160318-2 (Exp: 03/2019)
ASM4192017 (Exp: 04-2020)
Date Ranges: 03/2019, 04-2020

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 80241
Status: Active
Manufacturer: Absonutrix
Manufactured In: United States
Units Affected: 78/2 fl oz bottles

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.