[Recalled] OSCOR ADELANTE BREEZEWAY 10F C90¿ S79CM D84CM Catalog # AB101078 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture. — Complaint that durin
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | OSCOR ADELANTE BREEZEWAY 10F C90¿ S79CM D84CM Catalog # AB101078 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture. |
|---|---|
| Brand / manufacturer | Oscor, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0805-2017 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 05 October 2016 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Complaint that during insertion of the dilator through the sheath a fragment of inner liner came out of the sheath prior to use.
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 →
Related recalls from Oscor, Inc.
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.