Performance Plus Marketing, Inc.

FDA Regulatory Profile

Performance Plus Marketing, Inc. appears in FDA public data with 7 recalls — including 7 Class I (most serious) —, 0 510(k) clearances, 1 FDA inspection, and 2 compliance actions on record. Its most recent recall (D-333-2013, Class I) was initiated on December 17, 2012.

Summary

Total Recalls
7 (7 Class I)
510(k) Clearances
0
Inspections
1
Compliance Actions
2

Recent Recalls

NumberClassProductDate
D-333-2013Class Ilibigrow XXXTREME Capsules, MAXIMUM STRENGTH FORMULA, 1000 mg, supplied in 1, 5 and 10 count blisterDecember 17, 2012
D-332-2013Class Ilibigrow capsules, PERFORMANCE ENHANCER, supplied in 1, 5 and 10 count blister packs, Distributed ByDecember 17, 2012
D-337-2013Class IMojo nights SUPREME Capsules, 1000 mg, Male Sexual Enhancer, supplied in 1 count blister packs, UPC December 17, 2012
D-334-2013Class IBLUE Diamond Pill, supplied in 1, 5 and 10 count blister packs, Male Sexual Enhancement, DistributedDecember 17, 2012
D-338-2013Class ICASANOVA Capsules, 450 mg, MALE SEXUAL ENHANCER, supplied i n1 count blister packs, UPC 736211906892December 17, 2012
D-336-2013Class IMojo nights Capsules, Male Sexual Enhancer, supplied in 1 and 5 count blister packs, Distributed By:December 17, 2012
D-335-2013Class IBLUE Diamond PLATINUM Capsules, 1000 mg, supplied in 1, 5 and 10 count blister packs, Distributed ByDecember 17, 2012