تسجيل الدخول
تسجيل جديد
الأحد - ذو الحجة 5, 1446
عن تيقظ
بحث عن منتج
تقديم بلاغ
أسئلة شائعة
تواصل معنا
EN
SA-16-02-25-788
التفاصيل
الرقم المرجعي
الشركة الصانعة
اسم الجهاز الطبي
Intubation ORAL/NASAL Endotracheal Tube
الأجهزة المتأثرة
Refer to Table 1: Affected Products(s) and Appendix A in the attachment.
الممثل المعتمد
AL MADAR MEDICAL SERVICES COMPANY
سبب المشكلة
Certain sizes of Intubation ORAL/NASAL Endotracheal Tube products may have a smaller diameter than expected.
الإجراء التصحيحي
- There is no need to remove an affected Endotracheal tube if it is already in use. However, please review the Instructions for Use with heightened awareness prior to continued use. - Check all inventory locations within your institution for the affected products listed in the attachment and discontinue use. - Destroy all affected products following your institution’s process for destruction. If destroying is not immediately possible at your facility, then the product should be quarantined until disposal. Manufacturer action: Instructions and Removal.
المرفقات
عودة للقائمة
