Class 2 Device Recall EvoTech Endoscope Cleaner & Reprocessor

• Date Initiated by Firm: February 13, 2008
• Date Posted: August 08, 2008
• Recall Status: Terminated on November 29, 2011
• Recall Number: Z-1368-2008
• Recall Event ID: 46906
• 510(K)Number: K061899 K040883
• Product Classification: Endoscope Washer/Disinfector - Product Code FEB
• Product: EvoTech Endoscope Cleaner & Reprocessor, Product ; Code 50004; Indicated for use with high level disinfectant CIDEX OPA Concentrate and an enzymatic detergent, CIDEZYME GI, to achieve cleaning and high level disinfection of heat sensitive semi-critical endoscopes.
• Code Information: Product Code 50004; Serial Numbers: 50004001070080, 50004001070082, 50004001070083, 50004001070043, 50004001070044, 50004001070046, 50004001070048, 50004001070023, 50004001070024, 50004001070021, 50004001070075, 50004001070045, 50004001070078, 50004001070079, 50004001070107, 50004001070110, 50004001070081, 50004001070062, 50004001070064, 50004001070063, 50004001070034, 50004001070025, 50004001070029, 50004001070047, 50004001070049, 50004001070061, 50004001070087, 50004001070088, 50004001070084, 50004001070077, 50004001070076, 50004001070085, 50004001070086, 50004001070090, 50004001070091, 50004001070094, 50004001070089, 50004001070092, 50004001070098, 50004001070097, 50004001070099, 50004001070100, 50004001070101, 50004001070105, 50004001070106, 50004001070108, 50004001070109, 50004001070102, 50004001070103, 50004001070104, 50004001070020, 50004001070031, 50004001070035, 50004001070036, 50004001070039, 50004001070042, 50004001070059, 50004001070065, 50004001070071, 50004001070072, 50004001070073, 50004001070074, 50004001070114
• Recalling Firm/ Manufacturer: Advanced Sterilization Products; 33 Technology Dr; Irvine CA 92618-2346
• For Additional Information Contact: Mizanu Kebede; 949-789-3922
• Manufacturer Reason for Recall: Cleaning cycles are being cancelled. Specific issues are: a) Water heater tank is rusting resulting in the in-line 0.2 micron filter prematurely clogging, b) Interface board malfunction resulting in a premature lid opening, and c) Minor fluid leaks within the system (commonly at the 0.2 micron filter attachment points).
• FDA Determined Cause: Other
• Action: Feburary 13, 2008 ASP issued an Urgent Product Recall Letter. ASP recommends that customers use an alternative reprocessing method until they return the system. However, if they do not have an alternate method for processing endoscopes and choose to continue using the EvoTech ECR System during this time, endoscopes processed through completed cycles in accordance with the User's Guide will be appropriately cleaned and highlevel disinfected. ASP is prepared to tailor an alternative solution to minimize the interruption to the customer's processing needs.
• Quantity in Commerce: 64 units
• Distribution: Worldwide Distribution --- including USA and countries of Canada and Japan.
• 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 = FEB and Original Applicant = ADVANCED STERILIZATION PRODUCTS