Kirkman Group Inc.
Kirkman Group Inc. appears in FDA public data with 7 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (F-1351-2014, Class II) was initiated on November 15, 2013.
Summary
- Total Recalls
- 7
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| F-1351-2014 | Class II | Maximum Spectrum EnZym-Complete/DPP-IV Fruit Free w/Isogest, Kirkman brand, Item # 0869A-120 and 093 | November 15, 2013 |
| F-1348-2014 | Class II | Chewable Maximum Spectrum EnZym-Complete/DPPIV with Isogest, Kirkmand brand. Item # 0893-090 | November 15, 2013 |
| F-1349-2014 | Class II | EnZym-Complete/DPP-IV II with Isogest, Kirkman brand. Item numbers: 0851A-090, 0851A-180, 0931-0 | November 15, 2013 |
| F-1352-2014 | Class II | Phenol Assist, Kirkman brand, Item # 0835-090 | November 15, 2013 |
| F-1353-2014 | Class II | Biofilm Defense, Kirkman brand, Item # 0881-060 and 5881-060 Biofilm Defense, Pure Compounding bra | November 15, 2013 |
| F-1350-2014 | Class II | Enzym-Complete/DPP-IV, Kirkman brand. Item numbers 0234-060, 0234-120, 0234-200, 5234-200 | November 15, 2013 |
| F-1347-2014 | Class II | Chewable EnZym-Complete/DPPIV with Isogest, Kirkman brand. Item # 0934-090. | November 15, 2013 |