Medical device recalls Moderate risk

Intuitive Surgical, Inc. recalls da Vinci S Surgical System IS2000, Patient-Cart Monitor Drape, 20 Pack. Microtek Medical Equipment Drapes are to be use…

Recall date
March 16, 2015
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1383-2015
FDA classification
Class II
Brand / firm
Intuitive Surgical, Inc.
Sold / distributed
Worldwide Distribution-Argentina, Australia, Austria, Belgium, Brazil, Bulgaria, Canada, Chile, China (including Hong Kong), Colombia, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Finland, France, France, Germany, Greece, Iceland, India, Indonesia, Ireland, Israel, Italy, Ja…

Why it was recalled

Cloudy/waxy appearance with potential to transfer waxy substance to the patient, and potential for drape to tear.

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

What was recalled

da Vinci S Surgical System IS2000, Patient-Cart Monitor Drape, 20 Pack. Microtek Medical Equipment Drapes are to be used to cover a variety of surgical and non-surgical equipment in various settings throughout the clinical setting.

Get recall alerts

Free email alert whenever Intuitive Surgical, Inc. has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Intuitive Surgical, Inc.