Asahi Kasei Medical Co., Ltd., Okatomi Plant: 7 recalls on record

Recalls filed with 1 agency: FDA (7).

First recall on record: September 26, 2012. Most recent: September 26, 2012.

Risk classification: Class II: 7

Most recent recalls

DateAgencyProduct
September 26, 2012FDAAsahi KASEI, REXEED(TM)- 18 LX, HEMODIALYZER dialysis filterZ-2424-2012
September 26, 2012FDAAsahi KASEI, REXEED(TM)- 25 SX, HEMODIALYZER dialysis filterZ-2421-2012
September 26, 2012FDAAsahi KASEI, REXEED(TM)- 21 SX, HEMODIALYZER dialysis filterZ-2420-2012
September 26, 2012FDAAsahi KASEI, REXEED(TM)- 13 LX, HEMODIALYZER dialysis filterZ-2422-2012
September 26, 2012FDAAsahi KASEI, REXEED(TM)- 15 SX, HEMODIALYZER dialysis filterZ-2418-2012
September 26, 2012FDAAsahi KASEI, REXEED(TM)- 15 LX, HEMODIALYZER dialysis filterZ-2423-2012
September 26, 2012FDAAsahi KASEI, REXEED(TM)- 18 SX, HEMODIALYZER dialysis filterZ-2419-2012

Questions about this company

How many recalls does Asahi Kasei Medical Co., Ltd., Okatomi Plant have?
Recalert has 7 U.S. recalls on record for Asahi Kasei Medical Co., Ltd., Okatomi Plant, published between September 26, 2012 and September 26, 2012.
What was the most recent Asahi Kasei Medical Co., Ltd., Okatomi Plant recall?
FDA recall Z-2424-2012, published September 26, 2012: Asahi KASEI, REXEED(TM)- 18 LX, HEMODIALYZER dialysis filter
Which agencies have handled Asahi Kasei Medical Co., Ltd., Okatomi Plant recalls?
Asahi Kasei Medical Co., Ltd., Okatomi Plant appears as the recalling firm in recalls from: FDA (7).

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