TransMotion Medical Inc recalls Powered stretcher chair used during facial and eye surgeries. One chair per package.

Recall date

November 14, 2014

Source

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

Recall number

Z-0996-2015

FDA classification

Class II

Brand / firm

TransMotion Medical Inc

Sold / distributed

Worldwide Distribution - US Distribution and the countries including Canada, Australia, Chile, China, Costa Rica, Germany, Algeria, Israel, Italy, South Korea, Malaysia, Nigeria, Netherlands, Poland, Portugal, Saudi Arabia, Singapore, Thailand, and Venezuela.

Why it was recalled

The firm is finding that the stretcher chair controllers are moving the chairs involuntarily.

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

What was recalled

Powered stretcher chair used during facial and eye surgeries. One chair per package.