First Source Inc recalls First Source iQ Flex M. Portable cart and platform that supports an X-ray system and laptop computer.

Recall date

May 9, 2024

Source

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

Recall number

Z-2247-2024

FDA classification

Class II

Brand / firm

First Source Inc

Sold / distributed

Worldwide - US Nationwide distribution in the states of AR, CA, FL, GA, IL, IN, LA, MA, MD, MI, MO, MS, NC, NY, OK, PA, TN, TX, & VA. The countries of Korea & Serbia.

Why it was recalled

Potential for the bolt that secures the positioning arm to the gas spring to come loose and fall onto patient.

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

What was recalled

First Source iQ Flex M. Portable cart and platform that supports an X-ray system and laptop computer.