PlainRecalls
FDA Devices Moderate Class II Terminated

Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone Screw Set.

Reported: February 8, 2017 Initiated: December 22, 2016 #Z-1113-2017

Product Description

Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone Screw Set.

Reason for Recall

The product is being recalled due to incidence and reports of the product breaking during surgery.

Details

Units Affected
N/A
Distribution
Distributed throughout the United States
Location
Horsham, PA

Frequently Asked Questions

What product was recalled?
Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone Screw Set.. Recalled by Flower Orthopedics Corporation. Units affected: N/A.
Why was this product recalled?
The product is being recalled due to incidence and reports of the product breaking during surgery.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 8, 2017. Severity: Moderate. Recall number: Z-1113-2017.