Class 1 Recall Issued for Ventlab's Manual Resuscitators

The FDA issued a Class 1 recall for Ventlab's adult and pediatric manual resuscitator, according to The Legal Examiner.

The manual resuscitators are used during patient transfers and as a back-up to anesthesia machines. The machines are said to have a defective valve, which can leak and prevent a patient from receiving oxygen or medication. The flaw is also hard to detect since the machine's bag deflates when it is compressed.

Affected resuscitators were manufactured and distributed between March and July 2012.

More Articles on Anesthesia:
Canton-Potsdam Develops Total Knee Replacement Pain Protocol
Spinal Anesthesia Reduces Risk in Total Knee Arthroplasty
Lower Dose of Dexamethasone Effective in Reducing Post-Operative Nausea




Copyright © 2024 Becker's Healthcare. All Rights Reserved. Privacy Policy. Cookie Policy. Linking and Reprinting Policy.

 

Featured Webinars

Featured Whitepapers

Featured Podcast