PlainRecalls
FDA Devices Moderate Class II Terminated

Extraction Hook - Sterile for TI Cannulated Nails

Reported: November 30, 2016 Initiated: October 3, 2016 #Z-0642-2017

Product Description

Extraction Hook - Sterile for TI Cannulated Nails

Reason for Recall

The peel pouches for the affected reaming rods and extraction hooks are delaminating.

Details

Units Affected
114 units
Distribution
Distributed Nationwide
Location
West Chester, PA

Frequently Asked Questions

What product was recalled?
Extraction Hook - Sterile for TI Cannulated Nails. Recalled by Synthes (USA) Products LLC. Units affected: 114 units.
Why was this product recalled?
The peel pouches for the affected reaming rods and extraction hooks are delaminating.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 30, 2016. Severity: Moderate. Recall number: Z-0642-2017.