Class IITerminated in FDA datasetNov 15, 2013

Enzym-Complete/DPP-IV, Kirkman brand. Item numbers 0234-060, 0234-120, 0234-200, 5234-200

Recalling firm: Kirkman Group Inc.

Why it was recalled

Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol

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Compare the exact product and package details with the label you have.

ProductEnzym-Complete/DPP-IV, Kirkman brand. Item numbers 0234-060, 0234-120, 0234-200, 5234-200

FDA code information

LOT numbers: 52587047, 52587048, 52587049, 52587050, 52588047, 52588048, 52588049, 52588050, 53853006, 53853007, 53853008, 53853009, 53853010, 54956000, 52588051,

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Full FDA record and distribution details

Original product description

Enzym-Complete/DPP-IV, Kirkman brand. Item numbers 0234-060, 0234-120, 0234-200, 5234-200

Extracted codes and context

TypeCode / valueContext
lot52587047LOT numbers: 52587047, 52587048, 52587049, 52587050, 52588047, 52588048, 52588049, 52588050, 53853006, 53853007, 53853008, 5385300
lot52587048LOT numbers: 52587047, 52587048, 52587049, 52587050, 52588047, 52588048, 52588049, 52588050, 53853006, 53853007, 53853008, 53853009, 5385301
lot52587049LOT numbers: 52587047, 52587048, 52587049, 52587050, 52588047, 52588048, 52588049, 52588050, 53853006, 53853007, 53853008, 53853009, 53853010, 5495600
lot52587050LOT numbers: 52587047, 52587048, 52587049, 52587050, 52588047, 52588048, 52588049, 52588050, 53853006, 53853007, 53853008, 53853009, 53853010, 54956000, 5258805
lot52588047LOT numbers: 52587047, 52587048, 52587049, 52587050, 52588047, 52588048, 52588049, 52588050, 53853006, 53853007, 53853008, 53853009, 53853010, 54956000, 52588051,
lot52588048LOT numbers: 52587047, 52587048, 52587049, 52587050, 52588047, 52588048, 52588049, 52588050, 53853006, 53853007, 53853008, 53853009, 53853010, 54956000, 52588051,
lot52588049T numbers: 52587047, 52587048, 52587049, 52587050, 52588047, 52588048, 52588049, 52588050, 53853006, 53853007, 53853008, 53853009, 53853010, 54956000, 52588051,
lot52588050 52587047, 52587048, 52587049, 52587050, 52588047, 52588048, 52588049, 52588050, 53853006, 53853007, 53853008, 53853009, 53853010, 54956000, 52588051,
lot52588051, 52588050, 53853006, 53853007, 53853008, 53853009, 53853010, 54956000, 52588051,
lot53853006, 52587048, 52587049, 52587050, 52588047, 52588048, 52588049, 52588050, 53853006, 53853007, 53853008, 53853009, 53853010, 54956000, 52588051,
lot53853007, 52587049, 52587050, 52588047, 52588048, 52588049, 52588050, 53853006, 53853007, 53853008, 53853009, 53853010, 54956000, 52588051,
lot53853008, 52587050, 52588047, 52588048, 52588049, 52588050, 53853006, 53853007, 53853008, 53853009, 53853010, 54956000, 52588051,
lot53853009, 52588047, 52588048, 52588049, 52588050, 53853006, 53853007, 53853008, 53853009, 53853010, 54956000, 52588051,
lot53853010, 52588048, 52588049, 52588050, 53853006, 53853007, 53853008, 53853009, 53853010, 54956000, 52588051,
lot54956000, 52588049, 52588050, 53853006, 53853007, 53853008, 53853009, 53853010, 54956000, 52588051,

Recall details

Recall number
F-1350-2014
Event ID
66879
FDA status
Terminated
Initiated
Nov 15, 2013
Reported
Jan 8, 2014
Classified
Jan 2, 2014
Terminated
Apr 2, 2014
Quantity
11944 bottles (5956 bottles in the US and 5988 bottles outside the US)
Location
Lake Oswego, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

distributed worldwide

FDA source record · F-1350-2014

Data updated September 16, 2026. View official FDA data ↗

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