PlainRecalls
FDA Devices Moderate Class II Terminated

Exactech Optetrak Logic CC 15mm Tibial Augment Screws

Reported: July 19, 2017 Initiated: April 7, 2017 #Z-2704-2017

Product Description

Exactech Optetrak Logic CC 15mm Tibial Augment Screws

Reason for Recall

Missing Screw in carton. Nine (9) serial numbers were identified as being inadvertently packaged as one per carton when two per carton are required.

Details

Recalling Firm
Exactech, Inc.
Units Affected
9 devices
Distribution
CA and NY.
Location
Gainesville, FL

Frequently Asked Questions

What product was recalled?
Exactech Optetrak Logic CC 15mm Tibial Augment Screws. Recalled by Exactech, Inc.. Units affected: 9 devices.
Why was this product recalled?
Missing Screw in carton. Nine (9) serial numbers were identified as being inadvertently packaged as one per carton when two per carton are required.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 19, 2017. Severity: Moderate. Recall number: Z-2704-2017.