[Recalled] Myriad handpiece Tissue morcellator — This recall has been initiated due to a defective component within the handpiec… | FDA 2014-02-24
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Myriad handpiece Tissue morcellator |
|---|---|
| Brand / manufacturer | Nico Corp. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2045-2016 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 24 February 2014 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: This recall has been initiated due to a defective component within the handpiece which will cause the handpiece to fail. The failure will result in the inability to cut tissue with the handpiece, rendering it non-functional. Should this failure occur, a replacement Myriad handpiece will be required. If a replacement handpiece is not available, alternate instrumentation for tissue removal will be necessary.
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 Nico 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.