FDADecember 22, 2016device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Terminated

Brands named

flower orthopedicsflower

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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