Flower Orthopedics Corporation: Medical Device Recall in 2017 - (Recall #: Z-1113-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: December 22, 2016

Date Posted: February 8, 2017

Recall Number: Z-1113-2017

Event ID: 76156

Reason for Recall:

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

Status: Terminated

Product Quantity: N/A

Code Information:

Device Listing: D267957

Distribution Pattern:

Distributed throughout the United States

Voluntary or Mandated:

Voluntary: Firm initiated