FDAJanuary 3, 2017device

Arthrex Shoulder Suspension Tower; Catalog Number: AR-1650-01 Product Usage: The Arthrex Lateral Decubitus Shoulder Positioner is intended to allow for the controlled manipulation of the arm and shoulder joint during arthroscopic surgical procedures.

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

The hazard

During use, there is a potential scenario which could allow the fastening screws attaching covers to come loose and potentially land in the sterile field causing a delay in surgery.

What to do

FDA enforcement status: Terminated

Brands named

allen medical systemsallenallen medical

Recall history

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

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