SNI Nitric Blast Sour Apple (SNI) – geranium extract concern (2012)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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.
Brand
Sni llc
Lot Codes / Batch Numbers
all codes and expiration dates
Products Sold
all codes and expiration dates
Sni llc is recalling SNI Nitric Blast Sour Apple 276gr (UPC ending in 5581) --- The product is a powder marketed in a 276 due to SNI, LLC is recalling certain Nitric Blast brand products that contain geranium extract as a dietary ingredient. This ingredient is also called, among. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
SNI, LLC is recalling certain Nitric Blast brand products that contain geranium extract as a dietary ingredient. This ingredient is also called, among other names, dimethylamylamine, 1,3-dimethylamylamine, DMAA or methylhexanamine (DMAA ).
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 13, 2026