PapaZen 3300 capsule, Proprietary Blend 1800mg, 1-capsule packets, distributed by FX Power San Diego, CA 92108, UPC 718122032587
Reported: December 13, 2017 Initiated: September 15, 2017 #D-0104-2018
Product Description
PapaZen 3300 capsule, Proprietary Blend 1800mg, 1-capsule packets, distributed by FX Power San Diego, CA 92108, UPC 718122032587
Reason for Recall
Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical Ingredients sildenafil, desmethyl carbodenafil and tadalafil.
Details
- Recalling Firm
- Gadget Island, Inc
- Units Affected
- 89 1-capsule packets
- Distribution
- Nationwide in the USA
- Location
- Newark, CA
Frequently Asked Questions
What product was recalled? ▼
PapaZen 3300 capsule, Proprietary Blend 1800mg, 1-capsule packets, distributed by FX Power San Diego, CA 92108, UPC 718122032587. Recalled by Gadget Island, Inc. Units affected: 89 1-capsule packets.
Why was this product recalled? ▼
Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical Ingredients sildenafil, desmethyl carbodenafil and tadalafil.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on December 13, 2017. Severity: Critical. Recall number: D-0104-2018.
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