Kirkman Group EnZym-Complete/DPP-IV II with Isogest Recall

Why it was recalled

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

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.

Lot numbers, UPCs & expiration codes

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

Where it was sold

distributed worldwide

What to do if you have this product

Compare the brand, size, and lot/UPC codes on your package with the codes above.
If it matches, don't eat it. Return it to the store for a refund or throw it away.
Wash surfaces and containers that touched the product.
If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number: F-1349-2014
Classification: Class II
Status: Terminated
Recall initiated: Nov 15, 2013
FDA report date: Jan 8, 2014
Quantity: 9486 bottles (5584 bottles in the US and 3902 bottles outside US)
Recall type: Voluntary: Firm initiated
Recalling firm: Kirkman Group Inc.

Original FDA data

Every field from FDA enforcement report F-1349-2014, exactly as published.

Show all FDA fields

City: Lake Oswego
State: OR
Status: Terminated
Country: United States
Event ID: 66879
Address: 6400 Rosewood St
Code information: Lot numbers: 52939039, 52939040, 52939042, 52939043, 53852011, 53852012, 53852013, 53852015, 53852016,
Postal code: 97035-5392
Report date: Jan 8, 2014
Product type: Food
Recall number: F-1349-2014
Classification: Class II
Recalling firm: Kirkman Group Inc.
Product quantity: 9486 bottles (5584 bottles in the US and 3902 bottles outside US)
Termination date: Apr 2, 2014
Reason for recall: Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
Voluntary / mandated: Voluntary: Firm initiated
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.
Distribution pattern: distributed worldwide
Recall initiation date: Nov 15, 2013
Initial firm notification: E-Mail
Center classification date: Jan 2, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1349-2014, published Jan 8, 2014. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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