Severity
Moderate
FDA Food recall · Reported August 19, 2015
All ASN brand products are recalled because it was ordered by the United States District Court for the District of Oregon. Products are also recalled due to misbranded, adulterat…
James G. Cole, Inc., dba ASN/Maxam Neutraceutics recalled ALL ASN products: The ASN products are in capsule or powdered form and bear the ASN label… - a moderate-severity action.
ALL ASN products: The ASN products are in capsule or powdered form and bear the ASN label… was recalled by James G. Cole, Inc., dba ASN/Maxam Neutraceutics in August 19, 2015. Reason: All ASN brand products are recalled because it was ordered by the United States District Court for the Distri…. Check the official notice for the remedy. Verify recall #F-2957-2015 with the FDA Food before acting.
The recall
James G. Cole, Inc., dba ASN/Maxam Neutraceutics issued this moderate-severity FDA Food recall-All ASN brand products are recalled because it was ordered by the United States District Court for the Distri….
Sourced from official FDA Food enforcement records. Verify recall #F-2957-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-2957-2015) was formally reported on August 19, 2015, with the manufacturer initiating the action on March 6, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. James G. Cole, Inc., dba ASN/Maxam Neutraceutics is listed as the recalling firm, operating out of Hood River, OR. Federal records list the affected scope as The firm did not provide.
The documented reason for this recall is: All ASN brand products are recalled because it was ordered by the United States District Court for the District of Oregon. Products are also recalled due to misbranded, adulterated, and unapproved new drugs because of … Distribution data in the federal record shows the product reached: nationwide. 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, 1 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 - 14,287 drugs & medications 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 moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
The firm did not provide
Related Recalls
6
1 from same agency
ALL ASN products: The ASN products are in capsule or powdered form and bear the ASN label. *********the List of ASN products***************************** AFINITY WHEY PROTEIN; DHEA; HUMAGRO Homeopathic Growth Hormone 4c; PHYTOBOL; TESTRX; TRIBESTRONE II;
All ASN brand products are recalled because it was ordered by the United States District Court for the District of Oregon. Products are also recalled due to misbranded, adulterated, and unapproved new drugs because of certain claims about their effects had not been approved by the FDA.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-2957-2015 |
| Date reported | August 19, 2015 |
| Date initiated | March 6, 2015 |
| Recalling firm | James G. Cole, Inc., dba ASN/Maxam Neutraceutics |
| Firm location | Hood River, OR |
| Affected scope | The firm did not provide |
| Distribution | nationwide |
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 August 19, 2015. 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.