Food recall: ALL MAXAM PRODUCTS: The Maxam product is used orally in spray form and bears the Maxam label. ********The List of MAXAM
FDA enforcement event 70694 is a food recall by James G. Cole, Inc., dba ASN/Maxam Neutraceutics of Hood River, OR, initiated 6 Mar 2015 and classified Class II, with 2 product records.
FDA defines Class II as 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. 46% of the 607 food enforcement events initiated in 2015 carry the same class.
Status: Terminated, terminated 14 Jul 2017. Initiation: fda mandated. This is the only enforcement event on this register for James G. Cole, Inc., dba ASN/Maxam Neutraceutics.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
James G. Cole, Inc., dba ASN/Maxam Neutraceutics, Hood River, OR.
Reason for recall
"All Maxam 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."
Distribution
"nationwide"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-2956-2015 | ALL MAXAM PRODUCTS: The Maxam product is used orally in spray form and bears the Maxam label. ********The List of MAXAM products********************************************** AD Nutritional Support for a Positive Outlook; AFX Nutritional Support for Healthy Cellular Function; ANANDA Nutritional Support for Emotional… | the firm did not provide | Class II | Terminated | 19 Aug 2015 |
| F-2957-2015 | 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; | The firm did not provide | Class II | Terminated | 19 Aug 2015 |
Context
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "All Maxam 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."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is 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.
Where was the product distributed?
FDA's distribution pattern field reads: "nationwide"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 14 Jul 2017. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.