Medical device recalls Moderate risk

Natus Manufacturing Limited recalls Natus Warmette Blanket Cabinet and Warmette Dual Cabinet The Natus Warmette Blanket Cabinet is designed to store and wa…

Recall date
October 15, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0951-2017
FDA classification
Class II
Brand / firm
Natus Manufacturing Limited
Sold / distributed
Worldwide Distribution - US including NJ, NC, TX, IL, VA, NY, FL, CA, MS, WA, IN, and MA. and Internationally to Canada and Costa Rica.

Why it was recalled

The fuse blows during initial power up or after a period of time. This results in a complete loss of power to the Cabinet and in some cases has resulted in the fuse cover for the power inlet melting slightly.

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

What was recalled

Natus Warmette Blanket Cabinet and Warmette Dual Cabinet The Natus Warmette Blanket Cabinet is designed to store and warm blankets and hospital linens; while, the Natus Warmette Dual Cabinet is designed to store and warm blankets and hospital linens in one compartment and fluids (irrigation and/or injection) in the other compartment within the storage times and warming temperatures recommended by the manufacturers of those items

Get recall alerts

Free email alert whenever Natus Manufacturing Limited has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Natus Manufacturing Limited