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Allen Medical Systems, Inc. recalls Arthrex Shoulder Suspension Tower; Catalog Number: AR-1650-01 Product Usage: The Arthrex Lateral Decubitus Shoulder
Recalled February 22, 2017 · FDA recall Z-1198-2017 · Allen Medical Systems
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. · FDA Class II
Units
112 devices
Sold at
US state of FL
Description
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.
Product
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.
Manufacturer(s)
Allen Medical Systems, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →