FDA Recalls Boston Scientific Expo 5F Cardiac Catheters Due to Delamination
Boston Scientific is recalling 8,575 Expo 5F Selective Angiographic Catheters due to polyurethane delamination that prevents guidewire advancement. The FDA Class I recall affects devices distributed worldwide.
- Product
- Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WRP (5PK), REF H74908526512; cardiac catheter
- Category
- Medical Device
- Distribution
- 0 states