| Subject: | Recall of Certain Lots of Shiley Tracheostomy Tubes |
| Category: | Food and Drug Administration (FDA)
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| Published: | Mon, 26 Apr 2010 - 06:00 am |
| Audience: Emergency medicine, Hospital Risk Managers The Food and Drug Administration (FDA) and Coviden have notified healthcare professionals of a recall of certain lots of Coviden's cuffed Shiley tracheostomy tubes and Custom/Specialty tracheostomy tubes due to the product's cuff not holding air as a result of leaks in the pilot balloon inflation assembly. With respect to the affected units, if a cuff does not hold air, ventilation will be adversely affected since the ability to... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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