[Recalled] The EKOS EkoSonic Control Unit is intended exclusively for use with the EkoSonic Endovascular Device and the EkoSonic MACH4 Endovascular Device. The EkoSonic Endovascular System consists of three main components: -a single
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | The EKOS EkoSonic Control Unit is intended exclusively for use with the EkoSonic Endovascular Device and the EkoSonic MACH4 Endovascular Device. The EkoSonic Endovascular System consists of three main components: -a single use EkoSonic Endovascular Device which is comprised of an Intelligent D |
|---|---|
| Brand / manufacturer | EKOS Corporation |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2148-2015 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 24 June 2015 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The Connector Interface Cable (CIC) was not recognized by the EkoSonic PT-3B control unit.
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 EKOS 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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