تسجيل الدخول
تسجيل جديد
الجمعة - محرم 9, 1447
عن تيقظ
بحث عن منتج
تقديم بلاغ
أسئلة شائعة
تواصل معنا
EN
SA-21-04-25-867
التفاصيل
الرقم المرجعي
الشركة الصانعة
اسم الجهاز الطبي
Patient Monitoring Devices and Wall Systems; Manual Blood Pressure Gauges and Cuffs
الأجهزة المتأثرة
Refer to the attachment.
الممثل المعتمد
Farouk Mamoun Tamer and Co
سبب المشكلة
The product is labeled “not made with natural rubber latex,” however, there is a latex-containing rubber band located around the product instructions for use (IFU).
الإجراء التصحيحي
Immediately locate the impacted products at your facility that are unopened. Follow the instructions in Attachment A to determine if your unopened products are affected and how to arrange for return as appropriate. Manufacturer Action: Removal.
المرفقات
عودة للقائمة
