Severity
Critical
FDA Food recall · Reported September 26, 2012
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 172.17…
Hocean Inc recalled Nitre powder. Brand "Selected Product", 4oz plastic bags, UPC 0 45027 97918 2. - a critical-severity action.
Nitre powder. Brand "Selected Product", 4oz plastic bags, UPC 0 45027 97918 2. was recalled by Hocean Inc in September 26, 2012. Reason: FDA analysis of the product found that the product consisted of mainly sodium nitrite. The product's label f…. Check the official notice for the remedy. Verify recall #F-2356-2012 with the FDA Food before acting.
The recall
Hocean Inc issued this critical-severity FDA Food recall-FDA analysis of the product found that the product consisted of mainly sodium nitrite. The product's label f….
Sourced from official FDA Food enforcement records. Verify recall #F-2356-2012 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-2356-2012) was formally reported on September 26, 2012, with the manufacturer initiating the action on May 25, 2012. It is classified under Critical severity (Class I), with a current status of Terminated. Hocean Inc is listed as the recalling firm, operating out of City Of Commerce, CA. Federal records list the affected scope as 50 cases with 100, 4-oz packages per case.
The documented reason for this recall is: 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 … Distribution data in the federal record shows the product reached: 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 …. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Critical
Affected scope
50 cases with 100, 4-oz packages per case
Related Recalls
6
2 from same agency
Nitre powder. Brand "Selected Product", 4oz plastic bags, UPC 0 45027 97918 2.
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.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-2356-2012 |
| Date reported | September 26, 2012 |
| Date initiated | May 25, 2012 |
| Recalling firm | Hocean Inc |
| Firm location | City Of Commerce, CA |
| Affected scope | 50 cases with 100, 4-oz packages per case |
| Distribution | 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 Virgin… |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported September 26, 2012. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.