تسجيل الدخول
تسجيل جديد
الخميس - جمادى الآخرة 25, 1446
عن تيقظ
بحث عن منتج
تقديم بلاغ
أسئلة شائعة
تواصل معنا
EN
SA-22-10-24-636
التفاصيل
الرقم المرجعي
الشركة الصانعة
اسم الجهاز الطبي
3M™ V.A.C.® Ulta Therapy Unit
الأجهزة المتأثرة
All Models and Serial Numbers
الممثل المعتمد
ALJEEL MEDICAL COMPANY
سبب المشكلة
A voluntary field corrective action on the occlusion detection sensor located on all models and serial numbers of the 3M™ V.A.C.® Ulta Therapy Unit.
الإجراء التصحيحي
1. Locate all serial numbers and Therapy Unit Software version of V.A.C.® Ulta Therapy Units. 2. Perform the steps outlined in the attached test procedure for the occlusion detection sensor 3. Record the test results on the provided Field Notice Receipt and Customer Response Form. Complete all remaining fields, sign and return this form via email to kci3mfieldactionresponse@solventum.com. Additional copies of the response form may be required based on the number of units in your facility. 4. For any therapy units with a “FAIL” test result, contact your Solventum representative to coordinate the repair/replacement of the occlusion detection sensor with your facility. If any additional issues are identified during the repair, you will be notified, and it will be the responsibility of the unit owner to determine whether to proceed with the additional services and associated costs.
المرفقات
عودة للقائمة
