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Terminated

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

FDA Recall Z-1113-2017 · Posted None

Recalling FirmFlower Orthopedics Corporation
Recall StatusTerminated
Product CodeLXH
Date Initiated2016-12-22
Date Terminated2017-11-27

Reason for Recall

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

Firm Action

Flower Orthopedics mailed a letter to customers on December 22, 2016 making them aware of the issue. Customers were asked to return the affected product and to report if any adverse effects resulted from its use.

Root Cause

Device Design

Distribution Pattern

Distributed throughout the United States

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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