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This is duplicated text of a letter from Baxter Corporation.
Contact the company for a copy of any references, attachments or enclosures.
October 05, 2007
Subject: RE: COLLEAGUE Triple Channel Mono, CX and CXE VOLUMETRIC INFUSION PUMPS. PRODUCT CODES: 2M8153, 2M8163, 2M9163, DNM 8153, and DNM9163
Dear Director of Biomedical Engineering or Director of Nursing:
Baxter Corporation is sending this Urgent Device Correction to inform you of an issue concerning the triple channel COLLEAGUE infusion pumps.
Baxter has recently received six (6) reports from 3 customers in Canada that COLLEAGUE triple channel infusion pumps stopped infusing during specific use conditions.
In each instance, the pump issued an audible and visual alert notification as designed, displayed a buffer overflow error code (16:310:867:0002) and stopped infusing. Of the reports received by Baxter, these interruptions occurred when the buffer memory capacity of the device was exceeded.
Our analysis has determined that the overall probability of buffer overflow is extremely unlikely. However, in a controlled laboratory environment, we were able to reproduce buffer overflow with a significantly higher probability of occurrence under the following specific use circumstances; when all three channels are simultaneously infusing fluid with both the dose mode and flow check enabled while either a dose mode titration is being performed or an alert is being resolved.
Baxter is currently validating a software solution to this issue and will provide it to customers once it has been completed.
Serious adverse consequences could occur if the pump stops infusing. Given this potential, Baxter requests that, in the interim, you immediately consider one of the following options to mitigate the occurrence of this interruption of therapy.
Single channel pumps are not affected by this issue and may be used as alternatives if available. If the mitigations outlined above are not acceptable, Baxter, subject to single channel pump availability, will provide you with single channel devices to be utilized as back up devices, as required.
Your Baxter representative will be in contact with you to answer any questions you may have or to coordinate the delivery of single channel pumps to your facility to serve as back-up devices should you feel they are required.
Please complete the attached reply form confirming your receipt of this letter and fax it to Baxter at the number provided on the form. Returning the form promptly will prevent you from receiving a repeat notice.
If you provide triple channel COLLEAGUE infusion pumps to other services or facilities, please forward this information to them immediately. It is imperative that all end users of the affected COLLEAGUE pumps be notified.
We sincerely apologize for any inconvenience this may cause you and your staff. If you have additional questions, please contact your Baxter Representative.
Health Canada has been notified of this action.
Sincerely,
original signed by
Pam Bobbette
Vice President, Quality
Baxter Corporation
FCA# 2001FCA14 COLLEAGUE and Baxter are registered trademarks of Baxter International, Inc.
Product Codes: 2M8153, 2M8163, 2M9163, DNM 8153, and DNM9163.
Customer Reply Form
(Urgent Device Correction letter dated October 05, 2007)
Please complete and return one copy of this form per facility to the FAX number listed below as confirmation that you have received this notification. A fax cover sheet is not required.
905-281-6420
We understand the contents of the letter and have disseminated this information to our staff and to other services or facilities, as applicable.
Signature/Date:
REQUIRED FIELD