Exactech Single Barrel Drill Guides The Single Barrel Drill Guide is… — Class II medical device recall Z-2071-2015
Terminated recall by Exactech, Inc., reported 2015-07-22, distributed nationwide. Shipped to a single consignee prior to completion of final inspection.
| Recall number | Z-2071-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Exactech, Inc., Gainesville, FL, United States |
| Recall initiated | 2015-05-21 |
| Classified | 2015-07-14 |
| Reported by FDA | 2015-07-22 |
| Terminated | 2015-07-16 |
| Distributed | Nationwide (US) |
| Quantity | 2 devices |
| Lot numbers | 68266001 |
| Model numbers | 05-109-14-0000 |
Product
Exactech Single Barrel Drill Guides The Single Barrel Drill Guide is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery.
Reason for recall
Shipped to a single consignee prior to completion of final inspection.
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-2071-2015. 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.