# FDA recall F-1112-2014

> **Global Health Laboratories, LLC** · Class II · food recall initiated 2013-11-07.

## 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 for recall

The finished dietary supplement product was manufactured with ingredients found to be contaminated with chloramphenicol, an antibiotic, above levels of 0.3 ppb.

## Distribution

Arizona

## Key facts

- **Recall number:** F-1112-2014
- **Recalling firm:** Global Health Laboratories, LLC
- **Classification:** Class II
- **Product type:** food
- **Status:** Terminated
- **Initiation date:** 2013-11-07
- **Report date:** 2013-12-25
- **Termination date:** 2017-03-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Amityville, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-1112-2014

## Citation

> AI Analytics. FDA recall F-1112-2014. Retrieved 2026-05-29 from https://api.ai-analytics.org/recall/F-1112-2014. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*