West Coast Laboratories Xambo Capsules Recall: Possible DMAA Contamination
West Coast Laboratories recalls 80 boxes of Xam: 12,053 capsules each, due to potential DMAA contamination. Consumers should check product details and contact the company for guidance.
Recall notice
West Coast Laboratories is recalling Xambo and Devagrass because there may be presence of 1,3-dimethylamylamine (DMAA).
Contact the company
What happened, in plain English
West Coast Laboratories is recalling 80 boxes of Xambo bulk capsules, each containing 12,053 capsules, because they may contain 1,3-dimethylamylamine (DMAA). This substance could pose health risks, so affected consumers should stop using the product and contact the manufacturer. Read more at govinfonow.com/recall/22426-west-coast-laboratories-xambo-capsules-recall-possible-dmaa-contamination.
Source Summary by GovInfoNow · govinfonow.com/recall/22426-west-coast-laboratories-xambo-capsules-recall-possible-dmaa-contamination · Updated October 8, 2026 · FDA enforcement record: FDA #F-1430-2017
Cite this page
“West Coast Laboratories Xambo Capsules Recall: Possible DMAA Contamination.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22426-west-coast-laboratories-xambo-capsules-recall-possible-dmaa-contamination. Based on FDA recall #F-1430-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1430-2017%22&limit=1).
Why it’s dangerous
DMAA is a stimulant that can cause health issues, including increased heart rate and blood pressure. The presence of DMAA in these capsules may lead to adverse health effects if consumed.
Who’s affected
Anyone who owns or uses the recalled Xambo capsules. People with health conditions that could be affected by DMAA are at higher risk.
How to tell if you have this one
Check for the product name 'Xambo' and the batch number 361215 on the packaging. The recall includes 80 boxes of bulk capsules, each containing 12,053 capsules.
- Brand
West Coast Laboratories- Category
Food
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Colombia, South America
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-1430-2017 | Xambo, 80 boxes of bulk capsules. Each containing 12,053 capsules in each box.; 361215 | 964,240 capsules |
| F-1431-2017 | Devagrass; Lot No. CK15005 Mfg. Lot no. 620815 | 3,600 blisters |
What to do — step by step
Check Product Details
Look for the product name 'Xambo' and batch number 361215 on the packaging to confirm if the item is recalled.
How this recall unfolded
Recall timeline
FDA terminated this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Similar recalls
Latest food recalls
Keep exploring
Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-1430-2017 (January 11, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1430-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.