FDA recall record
Nitre powder. Brand "Selected Product", 4oz plastic bags, UPC 0 45027 97918 2.
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of September 24, 2012. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Nitre powder. Brand "Selected Product", 4oz plastic bags, UPC 0 45027 97918 2.
Reason
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.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Nitre powder. Brand "Selected Product", 4oz plastic bags, UPC 0 45027 97918 2.
Code information listed by FDA
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.
Distribution and firm information
Recalling firm listed by FDA: Hocean Inc
Firm location listed by FDA: City Of Commerce, CA, United States
Distribution reported by FDA: 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.
Product quantity listed by FDA: 50 cases with 100, 4-oz packages per case
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.