Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Asahi KASEI Recalled by Asahi Kasei Medical Co., Ltd., Okatomi Plant Due to Asahi became aware of a negative trend for...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Asahi Kasei Medical Co., Ltd., Okatomi Plant directly.
Affected Products
Asahi KASEI, REXEED(TM)- 21 SX, HEMODIALYZER dialysis filter
Quantity: 30,408 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 1 state: TN
About Asahi Kasei Medical Co., Ltd., Okatomi Plant
Asahi Kasei Medical Co., Ltd., Okatomi Plant has 7 total recalls tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report