Sechrist Industries Inc recalls Sechrist Low Profile Wheeled Stretcher, Model No. 21762-110-33H, 21762-110-36H, 21762-110-41H, 21762-135-33HJ, 21762-01…

Recall date

June 1, 2015

Source

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

Recall number

Z-1939-2015

FDA classification

Class II

Brand / firm

Sechrist Industries Inc

Sold / distributed

US Distribution and Internationally to Japan and Jordan.

Why it was recalled

Sechrist Industries is recalling the Sechrist Low Profile Wheeled Stretcher because it may experience an unexpected incline angle during the height adjustment of the Low Profile Wheeled Stretcher when lifting the patient upward or when lowering the Wheeled Stretcher to a height at which the patient can be loaded/unloaded.

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

What was recalled

Sechrist Low Profile Wheeled Stretcher, Model No. 21762-110-33H, 21762-110-36H, 21762-110-41H, 21762-135-33HJ, 21762-010-36H, 21762-010-41H, 21762-111-36H.