| Subject: | Class I Recall of All Vampotherm 2001i Respiratory Gas Humidification Devices |
| Category: | Food and Drug Administration (FDA)
|
| Published: | Mon, 30 Jan 2006 - 10:00 am |
| Vapotherm, Inc., has initiated a nationwide Class I recall of all Vapotherm 2000i Respiratory Gas Humidification devices because some of these devices have been found to contain the Ralstonia species of bacteria.
Any healthcare facilities that have the Vapotherm 2000i device must return all devices to Vapotherm, Inc. Instructions for return of the device and a recall form are located the Vapotherm's recall website: http://www.vtherm.com/recall or may be obtained by calling Vapotherm, Inc. at... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
|
REFERENCE:
Policies / Forms / Additional Resources:
|
|
With over 20 years experience in regulatory compliance, MCN Healthcare brings you the most comprehensive regulatory compliance tool available. StayAlert! is the only comprehensive e-mail notification service available that not only notifies you of the changes in major federal regulations, but also provides the policies, procedures, tools and best practices to help you meet the changing regulation. StayAlert! actively monitors TJC (JCAHO), CDC, CMS, DHHS, FDA, OSHA, OIG and many others so you don't have to. The strength of StayAlert! rests in its ability to allow healthcare organizations to streamline their businesses using the Internet as a foundation architecture. StayAlert! provides cost containment and reduction through elimination of unnecessary overhead, and work caused by errors or poor access to information. |
|
