Total Digestion (Global Vitality) – Chloramphenicol risk (2013)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Total Digestion, Lot 1635, 4 boxes x 9.92 kg. Lot 1841, 4 boxes x 12 kg, 1 box x 11.24 kg. Lot 2017, 3 boxes x 10 kg, 1 box x 9.32 kg.
Brand
Global Vitality, Inc. dba Enzyme Process International
Lot Codes / Batch Numbers
Lot 1635, 1841, and 2017
Products Sold
Lot 1635, 1841, and 2017
Global Vitality, Inc. dba Enzyme Process International is recalling Total Digestion, Lot 1635, 4 boxes x 9.92 kg. Lot 1841, 4 boxes x 12 kg, 1 box x 11.24 kg. Lot 2 due to Global Vitality is recalling dietary supplements because they may be contaminated with chloramphenicol. The dietary supplements were made with a raw . This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Global Vitality is recalling dietary supplements because they may be contaminated with chloramphenicol. The dietary supplements were made with a raw ingredient that was on recalled by Specialty Enzymes & Biotechnologies due to chloramphenicol.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, HI, PA
Page updated: Jan 6, 2026