Stryker Medical Division of Stryker Corporation recalls Medi-Therm Hyper/Hypothermia System, MTA7900

Recall date

March 29, 2017

Source

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

Recall number

Z-2058-2017

FDA classification

Class II

Brand / firm

Stryker Medical Division of Stryker Corporation

Sold / distributed

USA (nationwide) Distribution and Internationally to Colombia.

Why it was recalled

The water may reheat too quickly if the unit is in "Automatic" mode, switched to "Manual" mode to view water temperature, and then switched back to "Automatic" mode.

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

What was recalled

Medi-Therm Hyper/Hypothermia System, MTA7900