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U.S. Department of Health and Human Services

Class 2 Device Recall Terumo Clirans Series E Excebrane Hollow Fiber Dialyzers

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  Class 2 Device Recall Terumo Clirans Series E Excebrane Hollow Fiber Dialyzers see related information
Date Initiated by Firm March 31, 2005
Date Posted May 03, 2005
Recall Status1 Terminated 3 on July 10, 2006
Recall Number Z-0791-05
Recall Event ID 31536
510(K)Number K003425  
Product Classification Dialyzer, High Permeability With Or Without Sealed Dialysate System - Product Code KDI
Product Terumo Clirans Series E Excebrane Hollow Fiber Dialyzers; a wet model single use dialyzer consisting of hollow fiber membranes (23 microns thick) of vitamin E coated copolymer cellulose housed within a polyurethane casing, filled at the factory with fluid to facilitate priming by the user, and sterilized by autoclaving before shipment; Terumo Corporation, Tokyo 151-0072, Japan; Terumo Medical Corporation, Somerset, NJ 08873 U.S.A.; Made in Japan, 24 units per case; Models CL*E12NLA - 1.2 m2 surface area, CL*E15NLA - 1.5 m2 surface area, CL*E18NLA - 1.8 m2 surface area and CL*E20NLA - 2.0 m2 surface area
Code Information Schein product code 629-9041, Model CL*E12NLA, lot numbers 040408, 0404080511, 040511, 0405110610, 040610, 040909; Schein product code 629-5978, Model CL*E15NLA, lot numbers 040406, 0404060511, 040511; Schein product code 629-1824, Model CL*E18NLA, lot numbers 031020, 0310201215, 031215; Schein product code 629-7278, Model CL*E20NLA, lot numbers 020604, 0206040711, 020711;
Recalling Firm/
Manufacturer		 Asahi Medical Co Ltd
1-1 Uchiauwaicho,1-Chome
14 Flr, Imperial Tower Bldg
Chiyoda Ku Japan
For Additional Information Contact Mr. Hiroshi Miyazaki
847-498-8500
Manufacturer Reason
for Recall		 Exposure to freezing temperatures may damage the hollow fiber dialyzers and result in blood leaks during dialysis.
FDA Determined
Cause 2		 Other
Action Asahi sent Henry Schein, Inc. a recall letter dated 3/30/05, requesting the recall of the affected lots of Asahi labeled product, and Henry Schein, Inc. recalled the Asahi labeled dialyzers by letter dated 3/31/05, with a copy of the Asahi 3/30/05 letter. The accounts were informed that the dialyzers may have been exposed to temperature variances during distribution, and werw requested to cease distribution/use of the specific lots listed and return them to Henry Schein for credit. The recall was expanded to include the Terumo labeled dialyzers distributed by Asahi by Henry Schein letter dated 4/13/05, accompanied by a Terumo letter dated 4/8/05, sent to the accounts via first class mail on 4/14/05. The instructions were the same as in the 3/31/05 letter. A revised letter dated 4/21/05 was sent on 4/25/05, correcting the Henry Schein product codes involved in the Terumo labeled product. Any questions were directed Asahi Kasei Medical Co. at 847-498-8500.
Quantity in Commerce 11, 240 units
Distribution Nationwide and Puerto Rico
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database 510(K)s with Product Code = KDI and Original Applicant = TERUMO MEDICAL CORP.
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