Asahi Kasei Medical Co., Ltd., Okatomi Plant
Asahi Kasei Medical Co., Ltd., Okatomi Plant 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 (Z-2424-2012, Class II) was initiated on September 21, 2012.
Summary
- Total Recalls
- 7
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-2424-2012 | Class II | Asahi KASEI, REXEED(TM)- 18 LX, HEMODIALYZER dialysis filter | September 21, 2012 |
| Z-2420-2012 | Class II | Asahi KASEI, REXEED(TM)- 21 SX, HEMODIALYZER dialysis filter | September 21, 2012 |
| Z-2418-2012 | Class II | Asahi KASEI, REXEED(TM)- 15 SX, HEMODIALYZER dialysis filter | September 21, 2012 |
| Z-2423-2012 | Class II | Asahi KASEI, REXEED(TM)- 15 LX, HEMODIALYZER dialysis filter | September 21, 2012 |
| Z-2419-2012 | Class II | Asahi KASEI, REXEED(TM)- 18 SX, HEMODIALYZER dialysis filter | September 21, 2012 |
| Z-2421-2012 | Class II | Asahi KASEI, REXEED(TM)- 25 SX, HEMODIALYZER dialysis filter | September 21, 2012 |
| Z-2422-2012 | Class II | Asahi KASEI, REXEED(TM)- 13 LX, HEMODIALYZER dialysis filter | September 21, 2012 |