H-1263-2026
ZMB Enterprises
Data retrieved 2026-10-27T22:06:49.008Z
Site-assigned category (for this product recall): Unapproved or unlawful ingredient
Independent website; not affiliated with or endorsed by FDA. Recall information is attributed to the linked FDA record. Categories are assigned by this website using keyword rules; they are not FDA classifications or independent legal findings and may be incomplete or incorrect. A category summarizes the stated reason for the identified product recall, not a finding about the firm generally or its other products. FDA’s original reason text appears below.
Official openFDA record · FDA recalls and safety alerts
Fields as reported by FDA
Dates are formatted YYYY-MM-DD. “Not reported” means the field was absent or empty.
- recall_number
- H-1263-2026
- event_id
- 98691
- recalling_firm
- ZMB Enterprises
- city
- Carlsbad
- state
- CA
- country
- United States
- product_description
- Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement
- reason_for_recall
- The product contains 1,4-DMAA, Phenylethylamine and Phenibut.
- classification
- Class I
- FDA-reported status (not current status)
- Ongoing
FDA does not update this status after recall classification. It may not reflect whether the recall is currently ongoing, completed, or terminated. - voluntary_mandated
- Voluntary: Firm initiated
- distribution_pattern
- The firm markets their products online via their website addallxr.com
- product_quantity
- unknown
- code_info
- Sold between July - December 2025
- recall_initiation_date
- 2026-04-03
- report_date
- 2026-09-02
- termination_date
- Not reported