ErgoSafe Products, LLC (DBA) Prism Medical recalls Carry bar which is an accessory to a lift used for patients in hospitals and other facilities. Recall impacts the follo…

Recall date

August 30, 2016

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0728-2017

FDA classification

Class II

Brand / firm

ErgoSafe Products, LLC (DBA) Prism Medical

Sold / distributed

Distributed US nationwide and to Canada, Japan, Australia, Thailand, Great Britain, and South Korea

Why it was recalled

The black plastic puck on the carry bar is breaking resulting in potential for patient harm.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Carry bar which is an accessory to a lift used for patients in hospitals and other facilities. Recall impacts the following model numbers: 360741, 360750, 360751, 360755, 360755 Rev B, 360756, and 360757.