Medical device recalls Moderate risk

Intuitive Surgical, Inc. recalls SEAL,IS4000 PORTS,5MM-8MM,BOX of 10; Model numbers: 470361-03, 470361-04, 470361-05, 470361-06; Part number: 470361. Th…

Recall date
May 9, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1836-2016
FDA classification
Class II
Brand / firm
Intuitive Surgical, Inc.
Sold / distributed
Worldwide distribution. US, Australia, Austria, Belgium, Chile, Cyprus, Czech Republic, Denmark, Finland, France, Germany, Hong Kong, India, Ireland, Israel, Italy, Japan, Monaco, Netherlands, Norway, Puerto Rico, Portugal, Qatar, Romania, Saudi Arabia, Singapore, South Korea, Spain, Sweden, Switze…

Why it was recalled

Potential for particulates in insufflation stopcocks on the da Vinci Xi Surgical System cannula seals. The particulates could be introduced into the cannula lumen when insufflation is connected during a surgical procedure.

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

What was recalled

SEAL,IS4000 PORTS,5MM-8MM,BOX of 10; Model numbers: 470361-03, 470361-04, 470361-05, 470361-06; Part number: 470361. The da Vinci Xi Surgical System cannula sterile single use disposable cap for each cannula . When attached to the cannula, the seal maintains insufflation when the cannula is empty and when the instrument is inserted in the patient during a surgical procedure.

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.