OneBode Flo Probiotic Supplements Recalled for Chloramphenicol Contamination
Global Health Laboratories is recalling OneBode Flo probiotic supplements found to contain chloramphenicol, an antibiotic, above permitted levels.
The agency’s classification
FDA (Food): Class II
Class II is 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.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically involves a reasonable probability of temporary or medically reversible health consequences. The hazard is antibiotic contamination without reported illnesses, fitting the criteria for a moderate severity score.
Plain-English summary
Global Health Laboratories, LLC is recalling specific lots of OneBode Flo probiotic enzyme digestive dietary supplements. The recall includes OneBode Flo daily (90 capsules), OneBode Flo for Family (360 capsules), and OneBode Flo daily sample packs (6 capsules). The affected products were manufactured in Chandler, Arizona, and distributed in Arizona.
The recall was initiated because the finished dietary supplement products were manufactured with ingredients contaminated with chloramphenicol, an antibiotic, at levels above 0.3 parts per billion (ppb). The specific lot numbers involved are 1262057, 1262058, 26813, 26813A, and 26813B.
Consumers who have these products should stop using them and contact the recalling firm for further instructions. The source text does not specify a particular consumer action such as returning the product for a refund or disposal method, nor does it report any illnesses or injuries associated with the contamination.
The recalled product
- Product
- (a) ONEBODE Flo daily, probiotic enzyme digestive, 90 capsules, dietary supplement, Product No. T00135, UPC 0 14834 00135 5; (b) ONEBODE Flo for Family, probiotic enzyme digestive, 360 capsules, dietary supplement, Product No. T00109, UPC 0 14834 00109 6; (c) ONEBODE Flo daily…
- Manufacturer
- Global Health Laboratories, LLC
- Category
- Food — Dietary Supplement
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (5)
- (a) Lot Number 1262057
- (b) Lot Number 1262058
- (c) Lot Numbers 26813
- 26813A
- 26813B
Distribution
Distributed in 1 state:
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