Karman Healthcare Inc recalls Karma Flexx Wheelchair Manual Wheelchair.

Recall date

January 27, 2016

Source

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

Recall number

Z-1025-2016

FDA classification

Class II

Brand / firm

Karman Healthcare Inc

Sold / distributed

U.S. distribution to the following states -- WA, CA, NY, and TX.

Why it was recalled

Karman Healthcare, Inc. is recalling Karma Flexx Wheelchair because incorrect size screws and corresponding hardware were installed on the front caster fork brackets.

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

What was recalled

Karma Flexx Wheelchair Manual Wheelchair.