Devagrass
Recalling firm: West Coast Laboratories Inc
Why it was recalled
West Coast Laboratories is recalling Xambo and Devagrass because there may be presence of 1,3-dimethylamylamine (DMAA).
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 20, 2017.
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ProductDevagrass
FDA code information
Lot No. CK15005 Mfg. Lot no. 620815
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Full FDA record and distribution details
Original product description
Devagrass
Original FDA recall reason
West Coast Laboratories is recalling Xambo and Devagrass because there may be presence of 1,3-dimethylamylamine (DMAA).
Recall details
- Recall number
- F-1431-2017
- Event ID
- 76003
- FDA status
- Terminated
- Initiated
- Jan 11, 2017
- Reported
- Feb 8, 2017
- Classified
- Feb 1, 2017
- Terminated
- Mar 20, 2017
- Quantity
- 3,600 blisters
- Location
- Gardena, CA, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
Colombia, South America
FDA source record · F-1431-2017
Data updated September 16, 2026. View official FDA data ↗
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