PlainRecordsFDA · Drug recall
Pro Power Knight Plus capsule… and 2 more products
- Date
- May 10, 2023
- Risk class
- Class I (FDA's definition, 21 CFR 7.3(m): a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death)
- Status
- Ongoing
- Filed by
- Gadget Island, Inc
- Reason
- Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
- Distribution pattern
- Nationwide in the USA.
3 products in this recall
Pro Power Knight Plus capsule…
- Product
- Pro Power Knight Plus capsule, 2550mg, 1-count blister card, Distributed by Beyond Health and youth Inc, Seattle, WA 98110, UPC 4 94922 90522 0.
- Quantity
- 628 blister cards
- Codes and lots
- No lot number, Exp: 06/2026
- Recall started
- April 26, 2023
- Recall number
- D-0571-2023
NUX Male Enhancement capsule…
- Product
- NUX Male Enhancement capsule, 1-count blister card, distributed by SX Power CO., Chicago, Il 60612, UPC 6 01577 51236 3.
- Quantity
- 18 blister cards
- Codes and lots
- Lot#: RO 927996, Exp: 12/25/2024
- Recall started
- April 26, 2023
- Recall number
- D-0572-2023
DYNAMITE SUPER capsule…
- Product
- DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799 37602 7.
- Quantity
- 140 blister packs
- Codes and lots
- Lot/Item#: OMS760-B, Exp: 12/2025
- Recall started
- April 26, 2023
- Recall number
- D-0573-2023
What should I do? A baby or kids' product was recalled: what to do
Source: FDA · Drug enforcement reports, recall numbers D-0571-2023, D-0572-2023, D-0573-2023. The agency record governs; check it and the company before acting.