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Asahi Kasei Medical Co., Ltd., Okatomi Plant Recalls

7 recalls on record · September 26, 2012 to September 26, 2012 · Medical Devices

September 26, 2012Medical DevicesFDA
Asahi Kasei Medical Co., Ltd., Okatomi Plant recalls Asahi KASEI, REXEED(TM)- 18 LX, HEMODIALYZER dialysis filter
Hazard: Asahi became aware of a negative trend for rate of the adverse events that may be associated with a manufacturing change to certain lot numbers of the products, though there is no sufficient information to date to conclusively link these adverse events to the products.
September 26, 2012Medical DevicesFDA
Asahi Kasei Medical Co., Ltd., Okatomi Plant recalls Asahi KASEI, REXEED(TM)- 15 LX, HEMODIALYZER dialysis filter
Hazard: Asahi became aware of a negative trend for rate of the adverse events that may be associated with a manufacturing change to certain lot numbers of the products, though there is no sufficient information to date to conclusively link these adverse events to the products.
September 26, 2012Medical DevicesFDA
Asahi Kasei Medical Co., Ltd., Okatomi Plant recalls Asahi KASEI, REXEED(TM)- 13 LX, HEMODIALYZER dialysis filter
Hazard: Asahi became aware of a negative trend for rate of the adverse events that may be associated with a manufacturing change to certain lot numbers of the products, though there is no sufficient information to date to conclusively link these adverse events to the products.
September 26, 2012Medical DevicesFDA
Asahi Kasei Medical Co., Ltd., Okatomi Plant recalls Asahi KASEI, REXEED(TM)- 25 SX, HEMODIALYZER dialysis filter
Hazard: Asahi became aware of a negative trend for rate of the adverse events that may be associated with a manufacturing change to certain lot numbers of the products, though there is no sufficient information to date to conclusively link these adverse events to the products.
September 26, 2012Medical DevicesFDA
Asahi Kasei Medical Co., Ltd., Okatomi Plant recalls Asahi KASEI, REXEED(TM)- 21 SX, HEMODIALYZER dialysis filter
Hazard: Asahi became aware of a negative trend for rate of the adverse events that may be associated with a manufacturing change to certain lot numbers of the products, though there is no sufficient information to date to conclusively link these adverse events to the products.
September 26, 2012Medical DevicesFDA
Asahi Kasei Medical Co., Ltd., Okatomi Plant recalls Asahi KASEI, REXEED(TM)- 18 SX, HEMODIALYZER dialysis filter
Hazard: Asahi became aware of a negative trend for rate of the adverse events that may be associated with a manufacturing change to certain lot numbers of the products, though there is no sufficient information to date to conclusively link these adverse events to the products.
September 26, 2012Medical DevicesFDA
Asahi Kasei Medical Co., Ltd., Okatomi Plant recalls Asahi KASEI, REXEED(TM)- 15 SX, HEMODIALYZER dialysis filter
Hazard: Asahi became aware of a negative trend for rate of the adverse events that may be associated with a manufacturing change to certain lot numbers of the products, though there is no sufficient information to date to conclusively link these adverse events to the products.
Asahi Kasei Medical Co., Ltd., Okatomi Plant Recalls | RecallWatchUSA