Phenol Assist, Kirkman brand, Item # 0835-090
Recalled by Kirkman Group INC. on Nov 15, 2013
Recall Summary
Kirkman Group INC. recalled Phenol Assist, Kirkman brand, Item # 0835-090 in a Class II action, the FDA tier for products that may cause temporary or medically reversible health effects on Nov 15, 2013.
The FDA-published reason for this recall is: "Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol"
Distribution was limited; the FDA record lists "distributed worldwide." Single-area recalls still warrant a kitchen check for anyone who shops within that footprint. The recalling firm is based in Lake Oswego, OR. The recall covers 1774 bottles (1313 bottles in the US and 461 outside of the US) of product. The FDA has Terminated this recall (first reported Jan 8, 2014), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.
Reason for Recall
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
Product Description
Phenol Assist, Kirkman brand, Item # 0835-090
Distribution
distributed worldwide
What Should You Do?
- 1.Check your kitchen for this product immediately.
- 2.Do not consume the recalled product.
- 3.Return the product to where you bought it for a full refund, or throw it away.
- 4.If you have experienced any health issues, contact your healthcare provider.
Terms Explained
- Class II Recall — learn what this means in food safety
- FDA Food Recall — learn what this means in food safety
Source: FDA Recalls, Market Withdrawals and Safety Alerts, 2026.