CARTO VIZIGO Guiding Sheath Recalled Due to Water-Damaged Sterile Packaging
Biosense Webster is recalling 98 units of CARTO VIZIGO 8.5F guiding sheaths due to water damage to packaging that may have compromised the sterile barrier, creating a potential infection risk.
- Product
- CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath, REF: D138501. Used to introduce various cardiovascular catheters into the heart.
- Category
- Medical Device
- Distribution
- Distributed nationwide