(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

Global Health Laboratories, LLC recalled (a) ONEBODE Flo daily, probiotic enzyme digestive, 90 capsules, dietary supplement, Product No. T00135, UPC 0 14834 00135 5; (b) ONEBODE Flo in a Class II action, the FDA tier for products that may cause temporary or medically reversible health effects on Nov 7, 2013.

The FDA-published reason for this recall is: "The finished dietary supplement product was manufactured with ingredients found to be contaminated with chloramphenicol, an antibiotic, above levels of 0.3 ppb."

Distribution was limited; the FDA record lists "Arizona." Single-area recalls still warrant a kitchen check for anyone who shops within that footprint. The recalling firm is based in Amityville, NY. The recall covers Lot 1262057: 1985 bottles; Lot 1262058: 489 bottles; Sample packs: 11,276 units of product. The FDA has Terminated this recall (first reported Dec 25, 2013), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.