Recall Z-2663-2017— Exactech, Inc.
Class II · Terminated
Class II FDA medical device recall by Exactech, Inc., initiated 2017-05-25, terminated 2019-07-26. FDA's recall record names no specific 510(k) clearance for this event. Product: EXACTECH Equinoxe Reverse Starter Reamer - Catalog #: 321-05-01. Reason: 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..
- Recalling firm
- Exactech, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-05-25
- Terminated
- 2019-07-26
- Firm location
- Gainesville, FL, United States
Product description
EXACTECH Equinoxe Reverse Starter Reamer - Catalog #: 321-05-01
Reason for recall
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.