FDANovember 2, 2021device

Flex-Thread Inserter Shaft intended for Fibula intramedullary-intended to be used with the Inserter Draw Rod and Blue Ratchet Handle in order to facilitate the insertion of the Flex-Thread Nail System- Catalog Number: 8435-1

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

The hazard

Mating incompatibility between the Inserter Shaft and the Inserter Draw Rod causing the inserter draw rod to bind and not rotate freely as intended surgeon may be unable to complete surgery unless a second set is available

What to do

FDA enforcement status: Terminated

Brands named

flower orthopedicsflower

UPCs

00840118117548

Recall history

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

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