We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » Hamilton Ventilator Recall Deemed Class I for Software Issue Causing Device to Stop
Hamilton Ventilator Recall Deemed Class I for Software Issue Causing Device to Stop
The FDA has deemed Hamilton Ventilators’ recall of its C1, C2, C3, T1 ventilators as class I, as the company has received reports of software issues that may cause the ventilators to stop without notice, with the potential for serious injury or death.