Z-2071-2015 Class II Terminated
FDA device recall Z-2071-2015 was initiated by Exactech, Inc. on May 21, 2015 and is designated Class II. Reason for recall: Shipped to a single consignee prior to completion of final inspection. The recall status is terminated (terminated Jul 16, 2015). Affected quantity: 2 devices.
Recall Details
- Product Type
- Devices
- Report Date
- Jul 22, 2015
- Initiation Date
- May 21, 2015
- Termination Date
- Jul 16, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2 devices.
Product Description
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.
Distribution Pattern
Nationwide Distribution to Florida only.
Code Information
Catalog Number 05-109-14-0000, Lot # 68266001.
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2071-2015
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026