Schindele Enterprises dba Midwest Wholesale

FDA Regulatory Profile

Schindele Enterprises dba Midwest Wholesale appears in FDA public data with 7 recalls — including 7 Class I (most serious) —, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-1338-2014, Class I) was initiated on January 9, 2014.

Summary

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

Recent Recalls

NumberClassProductDate
D-1338-2014Class IMagic For Men, packaged in 1ct blister pack and 12-pill/bottle, 390 mg Manufactured For: BTQ Ski, IJanuary 9, 2014
D-1335-2014Class IBOOST ULTRA, sexual enhancement dietary supplement, 12-capsule/bottle. Also packaged in 3 pill bottJanuary 9, 2014
D-1340-2014Class IXZEN PLATINUM, 750 mg, Distributed by: XZEN, Los Angeles, CA.January 9, 2014
D-1337-2014Class IMiracleZEN Platinum, 1 pill blister pack, 2000 mg capsule, Distributed by: Power Life Distributors, January 9, 2014
D-1336-2014Class ISEXY MONKEY, 2000 mg, 1 count blister, Distributed by A Herbal Bio, Inc., Bayside, NY.January 9, 2014
D-1334-2014Class IXZONE GOLD, 1 capsule blister 750 mg, Distributed by: XZONE, Orlando, FL.January 9, 2014
D-1339-2014Class IExtenZe 600 mg, 30 tablet box, Manufactured for: Biotab Nutraceuticals, Inc., Pasadena, CA.January 9, 2014