Dymatize Enterprises, LLC

FDA Regulatory Profile

Dymatize Enterprises, LLC appears in FDA public data with 3 recalls — including 3 Class I (most serious) —, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (F-1230-2013, Class I) was initiated on May 3, 2012.

Summary

Total Recalls
3 (3 Class I)
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
F-1230-2013Class IDymatize Nutrition XPAND Post Xtreme Mass Recovery System Fruit Punch 3.5 lb Manufactured & DistribuMay 3, 2012
F-1229-2013Class IDymatize Nutrition XPAND Post Xtreme Mass Recovery System Lemonade 3.5 lb Manufactured & DistributedMay 3, 2012
F-1231-2013Class IDymatize Nutrition XPAND Post Xtreme Mass Recovery System Blue Raspberry 3.5 lb Manufactured & DistrMay 3, 2012