FDA recall record
DHEA 25mg, 60 count, sku: #6-09492-41001-6, and 90 count, sku: #6-09492-41002-3; 12 bottles/case.
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 December 11, 2015. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
DHEA 25mg, 60 count, sku: #6-09492-41001-6, and 90 count, sku: #6-09492-41002-3; 12 bottles/case.
Reason
Metabolic Response Modifiers (MRM) is recalling DHEA 25 mg capsules, 60 count and 90 count, because they may contain more DHEA than the label claims.
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.
DHEA 25mg, 60 count, sku: #6-09492-41001-6, and 90 count, sku: #6-09492-41002-3; 12 bottles/case.
Code information listed by FDA
lot numbers: 60-ct 140504 and 140802; and 90-ct 120640, 130764, 140113, 140227.
Distribution and firm information
Recalling firm listed by FDA: Chemi-source, Inc.
Firm location listed by FDA: Oceanside, CA, United States
Distribution reported by FDA: US
Product quantity listed by FDA: 5,977 units total
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.