[Recalled] Endurant II/IIs Stent Graft System: STENT GRAFT ETBF3216C145E ENDUR II BIF. For treatment of vascular aneurysms. — Incorrect stentstop assembly (18fr) was used to build the delivery system compo… | FDA 2021-04-28
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | Endurant II/IIs Stent Graft System: STENT GRAFT ETBF3216C145E ENDUR II BIF. For treatment of vascular aneurysms. |
|---|---|
| Brand / manufacturer | Medtronic Vascular, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1976-2021 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 28 April 2021 |
| EAN / barcode | 00613994990983 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Incorrect stentstop assembly (18fr) was used to build the delivery system component of the device. Correct stentstop assembly is 20fr.
This Class II 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
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
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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.