Xambo, 80 boxes of bulk capsules
Reason West Coast Laboratories is recalling Xambo and Devagrass because there may be presence of 1,3-dimethylamylamine (DMAA).
Devagrass recall
Recalled by West Coast Laboratories Inc · Gardena, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
West Coast Laboratories is recalling Xambo and Devagrass because there may be presence of 1,3-dimethylamylamine (DMAA).
The label gives no warning, so buyers cannot know about dangerous interactions with medicines they already take. All hidden drug ingredients recalls.
What was recalled
Devagrass
Quantity: 3,600 blisters
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot No. CK15005 Mfg. Lot no. 620815
Where it was sold
FDA's distribution note: Colombia, South America
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- West Coast Laboratories Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 11, 2017
- In FDA report of
- Feb 8, 2017
- Terminated
- Mar 20, 2017
- FDA recall number
- F-1431-2017 · event 76003
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.