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Global Health Laboratories, LLC
FDA recall F-1112-2014 · Class II · reported 2013-12-25 · Terminated
- 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, probiotic enzyme digestive, 6 capsules, dietary supplement (SAMPLE PACK), Product No. T00111, UPC 0 14834 00111 9 --- Mfg. for OneBode, Chandler, Arizona 85226
- Reason
- The finished dietary supplement product was manufactured with ingredients found to be contaminated with chloramphenicol, an antibiotic, above levels of 0.3 ppb.
- Quantity
- Lot 1262057: 1985 bottles; Lot 1262058: 489 bottles; Sample packs: 11,276 units
- Distribution
- Arizona
- Firm location
- NY, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Letter
- Recall started
- 2013-11-07
- Terminated
- 2017-03-10
- Code info
- (a) Lot Number 1262057; (b) Lot Number 1262058; (c) Lot Numbers 26813, 26813A, 26813B
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.