Global Health recalls ONEBODE Flo daily and family probiotic supplements due to chloramphenicol contamination above 0.3 ppb. Stop using if purchased between 2023-01-01 and 2023-01-01.
The finished dietary supplement product was manufactured with ingredients found to be contaminated with chloramphenicol, an antibiotic, above levels of 0.3 ppb.
Global Health is recalling ONEBODE Flo daily and family probiotic supplements because they were contaminated with chloramphenicol, an antibiotic, at levels above 0.3 ppb. This contamination could pose health risks if consumed.
Chloramphenicol is an antibiotic that can be harmful in high concentrations, potentially causing health issues when consumed in contaminated supplements. The contamination levels exceed the safe threshold of 0.3 ppb, which could pose risks to consumers.
People who purchased ONEBODE Flo daily, family, or sample packs between January 1, 2023, and January 1, 2023, are affected. Those with health conditions sensitive to antibiotics may be at higher risk.
Check for Product Numbers T00135 (daily), T00109 (family), or T00111 (sample) with Lot Numbers 1262057, 1262058, or 26813 series. The products were sold in the U.S. between January 1, 2023, and January 1, 2023.
Immediately stop using any recalled ONEBODE Flo products as they contain unsafe levels of chloramphenicol.
ONEBODE Flo daily (90 capsules, Product No. T00135), ONEBODE Flo for Family (360 capsules, Product No. T00109), and ONEBODE Flo daily sample packs (6 capsules, Product No. T00111).
Check for Product Numbers T00135, T00109, or T00111 with Lot Numbers 1262057, 1262058, or 26813 series. These were sold between January 1, 2023, and January 1, 2023.
The recall record does not specify a remedy, so consumers should stop using the products immediately.
We’ve drafted a message you can send ONEBODE to request your refund or repair — edit it as you like.
Subject: Recall F-1112-2014 — ONEBODE ONEBODE Hello, I own a ONEBODE that is covered by recall F-1112-2014 from ONEBODE. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
