FDAFDA · Food and drugs·Recall number Z-1658-2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL4.5 (5PK), REF H74908526232; cardiac catheter
Published May 22, 2024 · Recall initiated: March 21, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Boston Scientific Corporation
- Distributor
- Worldwide distribution. US, US Territories, EMEA, Canada, LATAM and Asia Pacific countries/regions.
- Lot
- UDI/DI 08714729187837, Batch Numbers: 60443928, 60457123, 60464496, 60473188, 60504888, 60522597, 60477305, 60517337, 60533589
- Risk classification
- Class I
- Area (FDA)
- device
- Country
- United States
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