Kirkman recalls Maximum Spectrum EnZym-Complete/DPP-IV Fruit Free supplements with possible chloramphenicol levels above 0.3 ppb. Consumers should check lot numbers 53854008-53854014 for affected items.
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
Kirkman is recalling certain Maximum Spectrum EnZym-Complete/DPP-IV Fruit Free supplements due to potential chloramphenicol contamination. This chemical, used in some antibiotics, can be harmful at very low levels and may pose health risks.
Chloramphenicol is an antibiotic that can be harmful at very low concentrations. The recalled supplements may contain levels above 0.3 ppb, which is a regulatory limit for safety. While the risk is low, it could cause health issues in sensitive individuals.
People who purchased Kirkman Maximum Spectrum EnZym-Complete/DPP-IV Fruit Free supplements with lot numbers 53854008, 53854010, 53854012, or 53854014 are affected. Those with health conditions requiring careful medication monitoring may be at higher risk.
Check the lot numbers on the product label: 53854008, 53854010, 53854012, or 53854014. The product is Kirkman Maximum Spectrum EnZym-Complete/DPP-IV Fruit Free w/Isogest with item numbers 0869A-120 or 0932-120.
Look for lot numbers 53854008, 53854010, 53854012, or 53854014 on the product label.
The recall states the product may contain chloramphenicol levels above 0.3 ppb, which could pose health risks. Kirkman has not provided specific safety instructions for use.
The recall does not specify a remedy, so no action is required beyond checking the product label for the lot numbers listed.
Check the lot numbers on the product label: 53854008, 53854010, 53854012, or 53854014.
We’ve drafted a message you can send Kirkman to request your refund or repair — edit it as you like.
Subject: Recall F-1351-2014 — Kirkman Kirkman Hello, I own a Kirkman that is covered by recall F-1351-2014 from Kirkman. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
