Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit — Class II medical device recall Z-0900-2017
Terminated recall by Exactech, Inc., reported 2016-12-28, distributed nationwide. Disengaged screw head could potentially not be retained in the Torque Defining Screwdriver.
| Recall number | Z-0900-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Exactech, Inc., Gainesville, FL, United States |
| Recall initiated | 2016-10-25 |
| Classified | 2016-12-22 |
| Reported by FDA | 2016-12-28 |
| Terminated | 2019-07-26 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BR, CA, CH, DE, ES, FR, GB, GR, GT, IN, IT, KR, LU, NL, SE, ZA |
| Quantity | 2,278 units |
| UPC / GTIN / UDI-DI | 10885862086518 |
| Model numbers | 320-20-00 |
Product
Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit
Reason for recall
Disengaged screw head could potentially not be retained in the Torque Defining Screwdriver.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0900-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.