[Recalled] Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK (5PKX3), REF H749085263002; cardiac catheter — An increase in complaints related to an inability to advance the guidewire thro… | FDA 2024-03-21
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK (5PKX3), REF H749085263002; cardiac catheter |
|---|---|
| Brand / manufacturer | Boston Scientific Corporation |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1666-2024 |
| Country of notice | United States |
| Risk level | Class I |
| Hazard type | recall |
| Notice date | 21 March 2024 |
| EAN / barcode | 08714729187868 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).
Read the full official notice →
Related recalls from Boston Scientific Corporation
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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