The Recall Desk

Hazard

Dmaa recalls

4 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
4
Critical
0
Severe
1
Most recent
2018-07-11

Of the 4 dmaa recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (25%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all dmaa recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–4 of 4

  • HighFDA (Food)·F-1604-2018·2018-07-11

    SNI Recalls Nitric Blast Products Containing Geranium Extract

    SNI, LLC is recalling Nitric Blast products containing geranium extract (DMAA) as a dietary ingredient.

    Product
    SNI Nitric Blast Sour Apple 276gr (UPC ending in 5581) --- The product is a powder marketed in a 276gr black bottle with a silver cap. The bottle prominently displays the product name "NITRIC BLAST" in silver and white letters on the front of a black label.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-2400-2014·2014-09-03

    Beta Labs Recalls PHEnFX Dietary Supplement Containing Unapproved DMAA

    Beta Labs is recalling 743 units of PHEnFX dietary supplements because they contain DMAA, a substance not permitted in dietary supplements.

    Product
    PHEnFX (TM), PHENO 550 mg, PHARMACEUTICAL GRADE, 90 CAPSULES, Manufactured for: Beta Labs, LTD, Newark, DE 19711, UPC 029882559802
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2398-2014·2014-09-03

    Beta Labs Recalls Oxyphen XR Fat Burner Due to Illegal DMAA Content

    Beta Labs is recalling Oxyphen XR fat burner capsules because they contain DMAA, a substance not permitted in dietary supplements.

    Product
    Oxyphen XR, 12 HR / CLINICAL STRENGTH FAT BURNER, 45 FAST ACTING EXTENDED RELEASE CAPSULES, Distributed by Beta Labs, LTD, Newark, DE 19711, UPC 670541599747
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1541-2014·2014-02-26

    YoungYou Recalls Mega Slim Herbal Appetite Management Due to DMAA

    YoungYou International is voluntarily recalling Mega Slim Herbal Appetite Management capsules because they contain DMAA.

    Product
    Mega Slim Herbal Appetite Management, 30 Capsules Bottle. Product labeling reads in part:"MEGASLIM Herbal Appetite Management***30 Capsules***YoungYou Weight Loss Center***MegaSim Propriety Blend 590 mg, Garcinia Cambogia Extract, Green Tea, Aloe Ferox, L-Carnitine, Caralluma
    Category
    Food
    Distribution
    0 states