Class ITerminated in FDA datasetMay 25, 2012

Nitre powder. Brand "Selected Product", 4oz plastic bags

Recalling firm: Hocean Inc

Why it was recalled

FDA analysis of the product found that the product consisted of mainly sodium nitrite. The product's label failed to bear adequate directions for use as required in 21 CFR 172.175. Failure to provide these directions for use may result in overuse that can pose an life-threatening hazard to health.

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The exact product

Nitre powder. Brand "Selected Product", 4oz plastic bags, UPC 0 45027 97918 2.

Check the codes

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Original FDA code information

The product does not bear any manufacturing codes. All product on the market at the time the recall was initiated on 5/25/2012 is subject to recall.

TypeCode / valueContext
UPC045027979182Nitre powder. Brand "Selected Product", 4oz plastic bags, UPC 0 45027 97918 2.

Recall details

Recall number
F-2356-2012
Event ID
61944
FDA status
Terminated
Initiated
May 25, 2012
Reported
Sep 26, 2012
Classified
Sep 20, 2012
Terminated
Sep 24, 2012
Quantity
50 cases with 100, 4-oz packages per case
Location
City Of Commerce, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

Distributed to wholesale distributors and Asian grocery stores nationwide to US states: California, Texas, Oregon, Nebraska, Georgia, Florida, Colorado, Oklahoma, Washington, New Mexico, Ohio, Arizona, Tennessee, North Carolina, and Virginia.

FDA source record · F-2356-2012

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.