FDASeptember 3, 2021device

Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201

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

The hazard

Product kit missing CDG 200 (Cannulated Countersink for 3.0-4.5mm Screws) from EWK 201 (Flower E-Kit, Advanced)

What to do

FDA enforcement status: Terminated

Brands named

flower orthopedicsflower

UPCs

00840118112079

Recall history

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

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