Diamond Shruumz Gummies recall

Recalled by Prophet Premium Blends, LLC · Santa Ana, CA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Toxic levels of muscimol

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

Diamond Shruumz Gummies - Micro Dose Grape Lemonade UPC 755003861584

Quantity: 248,007 products

Food: Chocolate & candy Juice & beverages

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

All lots or best buy dates and any products that do not have any lot codes or best buy dates.

Where it was sold

Alaska Alabama Arkansas Arizona California Colorado Connecticut District of Columbia Delaware Florida Georgia Hawaii Iowa Idaho Illinois Indiana Kansas Kentucky Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi Montana North Carolina North Dakota Nebraska New Hampshire New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania Puerto Rico Rhode Island South Carolina South Dakota Tennessee Texas Utah Virginia Vermont Washington Wisconsin West Virginia Wyoming

FDA's distribution note: U.S. distribution to the following: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY No foreign distribution.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm: Prophet Premium Blends, LLC
Initiated by: Voluntary: Firm initiated
Recall initiated: Jun 27, 2024
In FDA report of: Aug 7, 2024
Terminated: Apr 2, 2025
FDA recall number: F-1533-2024 · event 94869
Official record: FDA enforcement report search