Phenol Assist, Kirkman brand, Item # 0835-090
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1352-2014.
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1352-2014.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Kirkman Group Inc. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1352-2014.
Kirkman Group Inc.
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Kirkman Group Inc. Recall FAQ
Kirkman Group Inc. is the subject of a food safety report: Phenol Assist, Kirkman brand, Item # 0835-090. The notice was published on November 15, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 1,774 units are potentially affected.