EnZym-Complete/DPP-IV II with Isogest recall

Recalled by Kirkman Group Inc. · Lake Oswego, OR, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

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

Quantity: 9486 bottles (5584 bottles in the US and 3902 bottles outside US)

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

FDA's distribution note: distributed worldwide

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm: Kirkman Group Inc.
Initiated by: Voluntary: Firm initiated
Recall initiated: Nov 15, 2013
In FDA report of: Jan 8, 2014
Terminated: Apr 2, 2014
FDA recall number: F-1349-2014 · event 66879
Official record: FDA enforcement report search

Also recalled with it (6 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Other Nov 15, 2013