Severity
Critical
FDA Drug recall · Reported December 25, 2013
Marketed Without An Approved NDA/ANDA: New York State Department of Health analysis of this product found it to contain undeclared steroid-like substances making it an unapproved …
Healthy Life Chemistry Inc dba Purity First recalled Multi-Mineral capsules, 200-count bottles, labeled in part as Healthy Life Chemistry, By … - a critical-severity action.
Multi-Mineral capsules, 200-count bottles, labeled in part as Healthy Life Chemistry, By … was recalled by Healthy Life Chemistry Inc dba Purity First in December 25, 2013. Reason: Marketed Without An Approved NDA/ANDA: New York State Department of Health analysis of this product found it …. Check the official notice for the remedy. Verify recall #D-374-2014 with the FDA Drug before acting.
The recall
Healthy Life Chemistry Inc dba Purity First issued this critical-severity FDA Drug recall-Marketed Without An Approved NDA/ANDA: New York State Department of Health analysis of this product found it ….
Sourced from official FDA Drug enforcement records. Verify recall #D-374-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-374-2014) was formally reported on December 25, 2013, with the manufacturer initiating the action on July 31, 2013. It is classified under Critical severity (Class I), with a current status of Terminated. Healthy Life Chemistry Inc dba Purity First is listed as the recalling firm, operating out of Deer Park, NY. Federal records list the affected scope as unknown.
The documented reason for this recall is: Marketed Without An Approved NDA/ANDA: New York State Department of Health analysis of this product found it to contain undeclared steroid-like substances making it an unapproved new drug. Distribution data in the federal record shows the product reached: Approximately 30% of all finished products were sold to customers in interstate to include but may not be limited to NY, NJ & CT via UPS. Products are promoted and sold directly to customers at Healthy Life Chemistry's…. 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, 5 from FDA Drug - 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 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
unknown
Related Recalls
6
5 from same agency
Multi-Mineral capsules, 200-count bottles, labeled in part as Healthy Life Chemistry, By Purity First, Manufactured for: Purity First Health Products, Inc. Healthy Life Chemistry 51 Florida Street, Farmingdale, NY 11735; 1-800-696-7017
Marketed Without An Approved NDA/ANDA: New York State Department of Health analysis of this product found it to contain undeclared steroid-like substances making it an unapproved new drug.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | D-374-2014 |
| Date reported | December 25, 2013 |
| Date initiated | July 31, 2013 |
| Recalling firm | Healthy Life Chemistry Inc dba Purity First |
| Firm location | Deer Park, NY |
| Affected scope | unknown |
| Distribution | Approximately 30% of all finished products were sold to customers in interstate to include but may not be limited to NY, NJ & CT via UPS. Products are promoted and sold directly to customers at Healthy Life Chemistry's retail store at 13A… |
Profile values are sourced directly from the official FDA Drug 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 Drug 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 Drug, reported December 25, 2013. 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.