Food recall: Chewable EnZym-Complete/DPPIV with Isogest, Kirkman brand. Item # 0934-090.
Class II FDA enforcement event 66879. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Kirkman Group Inc. started this food recall on 15 Nov 2013. The firm address in the FDA record is in Lake Oswego, OR. FDA put the recall in Class II. FDA event 66879 has 7 product records. The first FDA enforcement report date is 8 Jan 2014. The record gives the status Terminated, with the termination date 2 Apr 2014.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
distributed worldwide
Recalling firm
Kirkman Group Inc., Lake Oswego, OR.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
7 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1347-2014 | Chewable EnZym-Complete/DPPIV with Isogest, Kirkman brand. Item # 0934-090. | 114 bottles (87 bottles in US and 27 bottles outside US) | Class II | Terminated | 8 Jan 2014 |
| F-1348-2014 | Chewable Maximum Spectrum EnZym-Complete/DPPIV with Isogest, Kirkmand brand. Item # 0893-090 | 79 bottles (43 bottles in US and 36 bottles outside US) | Class II | Terminated | 8 Jan 2014 |
| F-1349-2014 | EnZym-Complete/DPP-IV II with Isogest, Kirkman brand. Item numbers: 0851A-090, 0851A-180, 0931-090, 0931-180, 5851A-090, 5931-090. | 9486 bottles (5584 bottles in the US and 3902 bottles outside US) | Class II | Terminated | 8 Jan 2014 |
| F-1350-2014 | Enzym-Complete/DPP-IV, Kirkman brand. Item numbers 0234-060, 0234-120, 0234-200, 5234-200 | 11944 bottles (5956 bottles in the US and 5988 bottles outside the US) | Class II | Terminated | 8 Jan 2014 |
| F-1351-2014 | Maximum Spectrum EnZym-Complete/DPP-IV Fruit Free w/Isogest, Kirkman brand, Item # 0869A-120 and 0932-120. | 2273 bottles (1735 bottles in the US and 538 bottles outside the US) | Class II | Terminated | 8 Jan 2014 |
| F-1352-2014 | Phenol Assist, Kirkman brand, Item # 0835-090 | 1774 bottles (1313 bottles in the US and 461 outside of the US) | Class II | Terminated | 8 Jan 2014 |
| F-1353-2014 | Biofilm Defense, Kirkman brand, Item # 0881-060 and 5881-060 Biofilm Defense, Pure Compounding brand, Item # 1881-060. | 6099 bottles (5489 bottles in US and 610 outside the US) | Class II | Terminated | 8 Jan 2014 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Food events that started in 2013
- 546
- Share of these events in Class II
- 52%
- Product records in this event
- 7
- Events of the firm on the register
- 1
Official channels
- FDA enforcement report F-1347-2014The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
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Cite this page
Recall Register. FDA enforcement event 66879. https://recallregister.com/fda/ii/66879/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
distributed worldwide
- What quantity of product is in FDA event 66879?
- The event has 7 product records. The first record gives this quantity:
114 bottles (87 bottles in US and 27 bottles outside US)
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2013 have the same class?
- 52% of the 546 food events that started in 2013 are in Class II.