CareFusion Provides Update On Voluntary Recall Of EnVe Ventilator

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

CareFusion Provides Update On Voluntary Recall Of EnVe Ventilator

07/18/2012 03:42 PM EDT

CareFusion issued the following update regarding its previously announced voluntary recall of EnVe ventilators. The FDA has classified this action as a Class 1 recall.

. For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? support@govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 800-439-1420