Drug recall
Altrus Thermal Tissue Fusion Handpieces under the following specifications: 1) 10mm x 16 cm Catalog Number…
FDA recall event 67610 · Class II · ConMed Corporation
Key facts
| Event ID | 67610 |
|---|---|
| Recall numbers | Z-1839-2014 |
| Recalling firm | ConMed Corporation |
| Product type | Devices |
| Products | Altrus Thermal Tissue Fusion Handpieces under the following specifications: 1) 10mm x 16 cm Catalog Number: 60-9510-001, 2) 10 mm x 23 cm Catalog Number: 60-9511-001, 3) 10 mm x 36 cm Catalog Number… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | ConMed Corporation initiated an Urgent Medical Device Correction for Altrus Thermal Tissue Fusion Handpieces due to risk of burns. |
| Initiation date | Feb 20, 2014 |
| Report date | Jun 25, 2014 |
| Termination date | Apr 7, 2017 |
| City | Utica |
| State | NY |
| Country | United States |
| FEI number | 3001451571 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: