Class I
FDA
Addall XR Shot recalled over Unapproved ingredient
Older recall. This recall was announced about 7 months ago and the agency has not marked it resolved. We can't confirm its current status, so treat the official notice as authoritative — and note that shelf-stable products can stay in cupboards long after a recall is announced.
Addall XR Shot was recalled on April 3, 2026 because of unapproved ingredient. It is a Class I recall (reasonable probability of serious harm or death). Affected area: nationwide. Do not eat this product. Discard it or return it to the store for a refund.
HazardUnapproved ingredient
Risk levelClass I
Affected areaNationwide
CategoryFood
What to do
Do not eat this product. Discard it or return it to the store for a refund.
Confirm the details against the official FDA notice before acting.
Does this affect you?
Check the product in your home against the recalled item:
- Product as filed
- ZMB Enterprises — Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement
- Lot & date codes
- Sold between July - December 2025
Full recall details
- Reason for recall
- The product contains 1,4-DMAA, Phenylethylamine and Phenibut.
- Hazard class
- Class I — reasonable probability of serious harm or death
- Recalling company
- ZMB Enterprises
- Recall type
- Voluntary: Firm initiated
- Quantity
- unknown
- Distribution
- The firm markets their products online via their website addallxr.com
Compiled from the official FDA record by our data rules — how we build these pages. Spotted an error? Report it.
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