Gadget Island recalls

Gadget Island has 7 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 10 May 2023. 3 are still ongoing. The most frequent reason is labeling errors.

Total recalls7since 2017

Last 12 months0reported

Class I7100% of total

Ongoing3latest 10 May 2023

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 7 100%Class II 0 0%Class III 0 0%

Why gadget island is recalled

Labeling Errors7100%

By year

2023343%
2017457%

Ongoing gadget island recalls

3 active

Reported	Class	Recall	Company	Reason	Where
10 May 2023Drug	CLASS I	NUX Male Enhancement capsule blister card recalled by Gadget Island	Gadget Island	Labeling Errors	Nationwide
10 May 2023Drug	CLASS I	Pro Power Knight Plus capsule, 2550mg blister card recalled	Gadget Island	Labeling Errors	Nationwide
10 May 2023Drug	CLASS I	Dynamite Super capsule, 58,000 MG blister card recalled by Gadget Island	Gadget Island	Labeling Errors	Nationwide

All gadget island recalls, newest first

7 total

Reported	Class	Recall	Company	Reason	Where
10 May 2023Drug	CLASS I	NUX Male Enhancement capsule blister card recalled by Gadget Island	Gadget Island	Labeling Errors	Nationwide
10 May 2023Drug	CLASS I	Pro Power Knight Plus capsule, 2550mg blister card recalled	Gadget Island	Labeling Errors	Nationwide
10 May 2023Drug	CLASS I	Dynamite Super capsule, 58,000 MG blister card recalled by Gadget Island	Gadget Island	Labeling Errors	Nationwide
13 Dec 2017Drug	CLASS I	Rhino 7 Platinum, Proprietary Material: 750mg packets recalled	Gadget Island	Labeling Errors	Nationwide
13 Dec 2017Drug	CLASS I	PapaZen, Proprietary Blend 1800mg packets recalled by Gadget Island	Gadget Island	Labeling Errors	Nationwide
13 Dec 2017Drug	CLASS I	Fifty Shades, Proprietary Raw Material 4550 packets recalled	Gadget Island	Labeling Errors	Nationwide
13 Dec 2017Drug	CLASS I	grande X, (Maca Root 120 mg, Horny Goat Weed 120 mg recalled	Gadget Island	Labeling Errors	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.