Blue Fusion Capsules, 1- count blister pack, Distributed by: DNS Distribution 5225 Canyon Crest Dr. Ste 71-640, Riverside, CA 92507, UPC 7 48252 66460 0
Reported: April 3, 2019 Initiated: March 14, 2019 #D-1085-2019
Product Description
Blue Fusion Capsules, 1- count blister pack, Distributed by: DNS Distribution 5225 Canyon Crest Dr. Ste 71-640, Riverside, CA 92507, UPC 7 48252 66460 0
Reason for Recall
Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared ingredients: Sildenafil, Tadalafil, desmethyl carbodenafil, dithiodesmethyl carbodenafil, scutellarin, and daidzein.
Details
- Recalling Firm
- Ata International Inc
- Units Affected
- Unknown
- Distribution
- Nationwide within the United States
- Location
- Orange, CA
Frequently Asked Questions
What product was recalled? ▼
Blue Fusion Capsules, 1- count blister pack, Distributed by: DNS Distribution 5225 Canyon Crest Dr. Ste 71-640, Riverside, CA 92507, UPC 7 48252 66460 0. Recalled by Ata International Inc. Units affected: Unknown.
Why was this product recalled? ▼
Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared ingredients: Sildenafil, Tadalafil, desmethyl carbodenafil, dithiodesmethyl carbodenafil, scutellarin, and daidzein.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 3, 2019. Severity: Critical. Recall number: D-1085-2019.
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