Magic For Men Recalled for Undeclared Sildenafil and Tadalafil
Schindele Enterprises is recalling Magic For Men dietary supplements because they contain undeclared sildenafil and tadalafil without FDA approval.
What this means for you
Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.
Our severity reasoning: The agency classification is FDA Class I, which mandates a severity score of 5 according to the rubric.
Plain-English summary
Schindele Enterprises dba Midwest Wholesale is recalling Magic For Men dietary supplements, manufactured for BTQ Ski, Inc. The product is available in 1-count blister packs and 12-pill bottles, with a strength of 390 mg. The recall involves 59 1-count blister packs and 97 12-count bottles.
The recall was initiated because the dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil. These products were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). The affected lots include 12-count bottles with Lot GP808 (Expiration 10/16) and 1-count blisters with Lot BN030613 (Expiration 020615).
The products were distributed to Pennsylvania, Illinois, Texas, Iowa, Georgia, Connecticut, Florida, California, Louisiana, New York, Maryland, Nevada, and Wisconsin. Consumers should stop using the product and contact the manufacturer for a refund or further information.
The recalled product
- Product
- Magic For Men, packaged in 1ct blister pack and 12-pill/bottle, 390 mg Manufactured For: BTQ Ski, Inc., Chicago, IL 60638
- Manufacturer
- Schindele Enterprises dba Midwest Wholesale
- Category
- Drug — Dietary Supplement
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (5)
- 12-ct.bottle
- Lot GP808
- Exp. 10/16
- 1-ct. blister Lot BN030613
- EXP 020615
Distribution
Part of a larger recall action
This product is one of 7 recalled by Schindele Enterprises dba Midwest Wholesale under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 7 products in this recall →Related recalls
Same manufacturer · Schindele Enterprises dba Midwest Wholesale
See all →- CriticalDietary Supplement Recalled for Undeclared Sildenafil and Tadalafil Analogs
FDA (Drugs) · 2014-05-28
- CriticalXZONE GOLD Dietary Supplement Recalled for Undeclared Sildenafil and Tadalafil
FDA (Drugs) · 2014-05-28
- SevereMiracleZEN Platinum Recalled for Undeclared Sildenafil and Tadalafil
FDA (Drugs) · 2014-05-28
- CriticalExtenZe 600 mg Recalled for Undeclared Sildenafil and Tadalafil
FDA (Drugs) · 2014-05-28
- CriticalBoost Ultra Supplement Recalled for Undeclared Sildenafil and Tadalafil
FDA (Drugs) · 2014-05-28
Same hazard · undeclared ingredient
See all →- ModerateWise Onion Rings recalled for undeclared food color additives
FDA (Food) · 2026-07-15
- ModerateDietary supplement Ocular Plus recalled for undeclared Yellow #5
FDA (Food) · 2026-07-08
- ModerateDietary Supplement Vista MAX Recalled for Undeclared Yellow #5 Allergen
FDA (Food) · 2026-07-08
- ModerateEl David Gelee Bonbons Recalled for Undeclared Color Additives
FDA (Food) · 2026-07-01
- HighAdndale magnesium glycinate gummies contain undeclared melatonin in three lots
FDA (Food) · 2026-06-24