[Recalled] C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System — The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not me… | FDA 2019-10-21
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System |
|---|---|
| Brand / manufacturer | Integra LifeSciences Corp. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0639-2020 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 21 October 2019 |
| EAN / barcode | 60905781 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not meet the Dry Time Criteria for a 30-minute drying cycle. The current CUSA Clarity Operators manual states 30 minutes for the minimum Dry Time for the 36 kHz Sterilization Tray and 36 kHz Components but 40 minutes is required for complete drying.
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 Integra LifeSciences Corp.
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.