Exactech, Inc. recalls Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit
- Recalling company
- Exactech, Inc.
- Product
- Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit Model/Catalog Number: KIT-311X
- Reason
- Impactor handle may be missing cross-pin
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Feb 3, 2026
- Reported
- Mar 18, 2026
- Distribution
- US: CA CO FL GA HI ID IL IN KS KY LA MA MD ME MN NV NY OH OK PR SC TN TX VA WI OUS: Australia France Germany Italy Japan Korea Spain Switzerland United Kingdom United Arab Emirates Slovenia
- Status
- Ongoing
- Quantity
- 596 kits
- Lot / codes
- All Lots/ UDI-DI: 10885862559166
- Company location
- Gainesville, FL
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1510-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1510-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.