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Flower Orthopedics Corporation recalls Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone Screw Set.
Recalled February 8, 2017 · FDA recall Z-1113-2017 · Flower Orthopedics
Hazard
The product is being recalled due to incidence and reports of the product breaking during surgery. · FDA Class II
Units
N/A
Sold at
Distributed throughout the United States
Description
The product is being recalled due to incidence and reports of the product breaking during surgery.
Product
Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone Screw Set.
Manufacturer(s)
Flower Orthopedics Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →