Class II — Potential Health Hazard

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...

Date: September 21, 2012
Company: Asahi Kasei Medical Co., Ltd., Okatomi Plant
Status: Terminated
Source: FDA (Device)

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)- 15 LX, HEMODIALYZER dialysis filter

Quantity: 24 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

Affected (1 state)Not affected

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

Asahi Kasei Medical Co., Ltd., Okatomi Plant has 7 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report