Caesarea Medical Electronics Ltd

Syringe Driver

T34 Appendix 1 -Addendum to Instructions for Use Oct 2019

Addendum to Instructions for Use

11 Pages

The Chief Executive Officer URGENT PRODUCT DEFECT CORRECTION Caesarea Medical Electronics T34 Syringe Pumps Serial numbers: All serial numbers ARTG No: 131232 TGA Ref. No.: RC-2019-RN-01425-1 Product defect reason: The manufacturer, BD/CME has issued this Urgent Product Defect Correction to inform users of the T34™ Ambulatory Syringe Pump of an update to the Instructions for Use (IFU) and the Technical Service Manual to include revised inspection and cleaning practices for these pumps. Through customer feedback BD/CME has identified that there is a potential for fluid to ingress into the T34™ pump from routine cleaning and disinfection, which could over time, depending on the cleaning practice used, result in damage to the pump components, leading to potential impact on pump performance. As a result of this, BD/CME is revising the “Manufacturer Recommended Cleaning” instructions in the IFU (Appendix 1) and is updating the Technical Service Manual to include instructions for preventive maintenance (Appendix 2) to limit cumulative effects of fluid ingress over time. This notification is to make you aware of these changes and to provide copies of these revised instructions to be used with your pumps. Refer to Appendix 1 and Appendix 2. Please note that there is no requirement for customers to return or discontinue use of the T34™ Ambulatory Syringe Pumps. Action to be taken: 1. Read and distribute this Urgent Product Defect Correction Notice and ensure that all the contents are understood by those within your organisation and/or service organisation who need to be aware. 2. Attach Appendix 1 to the current IFU for your pumps and ensure its contents are made available to users that complete routine cleaning and disinfection practices for the T34™ pump. 3. Attach Appendix 2 to the current Technical Service Manual for your pumps and ensure its contents are made available to those in your organisation that perform the servicing/or your service provider. The guidance provided in the Technical Service Bulletin should be implemented and used at the next scheduled service/routine maintenance for the pumps. 4. Complete the attached acknowledgment form and return via email whether or not you have affected product, as we are required to confirm receipt of this notification from you. 5. If any of the stock could have been transferred from your facility to another, please immediately let that facility know of this notice and also notify REM SYSTEMS. Page 1 of 11
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File Name: Caesarea Medical Electronics Ltd - T34 Appendix 1 -Addendum to Instructions for Use Oct 2019 - 2019-10.pdf

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