[Recalled] EXACTECH Equinoxe Modular Reverse Pilot-Tip Reamer, Catalog #: 321-25-38, Catalog #: 321-25-42 and Catalog #: 321-25-46 — Instructions for use (IFU) is updated to clarify the proper technique and instr… | FDA 2017-05-25
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | EXACTECH Equinoxe Modular Reverse Pilot-Tip Reamer, Catalog #: 321-25-38, Catalog #: 321-25-42 and Catalog #: 321-25-46 |
|---|---|
| Brand / manufacturer | Exactech, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2666-2017 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 25 May 2017 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Instructions for use (IFU) is updated to clarify the proper technique and instrumentation to ream the Glenoid, i.e., to include a caution statement that the surgeon should ream on-axis and that reaming off-axis may result in instrument breakage.
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 →
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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.