Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported December 25, 2013
(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
The finished dietary supplement product was manufactured with ingredients found to be contaminated with chloramphenicol, an antibiotic, above levels of 0.3 ppb.
Compiled from official public sources by the editorial team.
Verify with FDA Food →
Global Health Laboratories, LLC recalled (a) ONEBODE Flo daily, probiotic enzyme digestive, 90 capsules, dietary supplement, Produ… - a moderate-severity action.
(a) ONEBODE Flo daily, probiotic enzyme digestive, 90 capsules, dietary supplement, Produ… was recalled by Global Health Laboratories, LLC in December 25, 2013. Reason: The finished dietary supplement product was manufactured with ingredients found to be contaminated with chlor…. Check the official notice for the remedy. Verify recall #F-1112-2014 with the FDA Food before acting.
The recall
Global Health Laboratories, LLC issued this moderate-severity FDA Food recall-The finished dietary supplement product was manufactured with ingredients found to be contaminated with chlor….
- Moderate
- severity level
- Class II
- classification
- December 25, 2013
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1112-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1112-2014) was formally reported on December 25, 2013, with the manufacturer initiating the action on November 7, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Global Health Laboratories, LLC is listed as the recalling firm, operating out of Amityville, NY. Federal records list the affected scope as Lot 1262057: 1985 bottles; Lot 1262058: 489 bottles; Sample packs: 11,276 units.
The documented 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 data in the federal record shows the product reached: Arizona. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 1 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
Lot 1262057: 1985 bottles; Lot 1262058: 489 bottles; Sample packs: 11,276 units
Related Recalls
6
1 from same agency
Product description
(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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1112-2014 |
| Date reported | December 25, 2013 |
| Date initiated | November 7, 2013 |
| Recalling firm | Global Health Laboratories, LLC |
| Firm location | Amityville, NY |
| Affected scope | Lot 1262057: 1985 bottles; Lot 1262058: 489 bottles; Sample packs: 11,276 units |
| Distribution | Arizona |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-1112-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
(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. Recalled by Global Health Laboratories, LLC. Units affected: Lot 1262057: 1985 bottles; Lot 1262058: 489 bottles; Sample packs: 11,276 units.
Why was this product recalled? ▼
The finished dietary supplement product was manufactured with ingredients found to be contaminated with chloramphenicol, an antibiotic, above levels of 0.3 ppb.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on December 25, 2013. Severity: Moderate. Recall number: F-1112-2014.
Where was the recalled product distributed? ▼
Distribution: Arizona.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1112-2014) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported December 25, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.