Class IITerminated in FDA datasetRecall initiated Nov 15, 2013

EnZym-Complete/DPP-IV II with Isogest, Kirkman brand. Item numbers: 0851A-090, 0851A-180,…

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Apr 2, 2014.

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ProductEnZym-Complete/DPP-IV II with Isogest, Kirkman brand. Item numbers: 0851A-090, 0851A-180, 0931-090, 0931-180, 5851A-090, 5931-090.

FDA code information

Lot numbers: 52939039, 52939040, 52939042, 52939043, 53852011, 53852012, 53852013, 53852015, 53852016,

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Full FDA record and distribution details

Original product description

EnZym-Complete/DPP-IV II with Isogest, Kirkman brand. Item numbers: 0851A-090, 0851A-180, 0931-090, 0931-180, 5851A-090, 5931-090.

Extracted codes and context

TypeCode / valueContext
lot52939039Lot numbers: 52939039, 52939040, 52939042, 52939043, 53852011, 53852012, 53852013, 53852015, 53852016,
lot52939040Lot numbers: 52939039, 52939040, 52939042, 52939043, 53852011, 53852012, 53852013, 53852015, 53852016,
lot52939042Lot numbers: 52939039, 52939040, 52939042, 52939043, 53852011, 53852012, 53852013, 53852015, 53852016,
lot52939043Lot numbers: 52939039, 52939040, 52939042, 52939043, 53852011, 53852012, 53852013, 53852015, 53852016,
lot53852011Lot numbers: 52939039, 52939040, 52939042, 52939043, 53852011, 53852012, 53852013, 53852015, 53852016,
lot53852012Lot numbers: 52939039, 52939040, 52939042, 52939043, 53852011, 53852012, 53852013, 53852015, 53852016,
lot53852013t numbers: 52939039, 52939040, 52939042, 52939043, 53852011, 53852012, 53852013, 53852015, 53852016,
lot53852015 52939039, 52939040, 52939042, 52939043, 53852011, 53852012, 53852013, 53852015, 53852016,
lot53852016, 52939040, 52939042, 52939043, 53852011, 53852012, 53852013, 53852015, 53852016,

Original FDA recall reason

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

Recall details

Recall number
F-1349-2014
Event ID
66879
FDA status
Terminated
Initiated
Nov 15, 2013
Reported
Jan 8, 2014
Classified
Jan 2, 2014
Terminated
Apr 2, 2014
Quantity
9486 bottles (5584 bottles in the US and 3902 bottles outside 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-1349-2014

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

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