| Subject: | Class 1 Recall Of Sun Med Greenline D MacIntosh No. 3 Laryngoscope Blades |
| Category: | Food and Drug Administration (FDA)
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| Published: | Fri, 19 Dec 2008 - 01:00 pm |
| The FDA has announced a Class I Recall of Sun Med Greenline/D MacIntosh No. 3 Sterile and Disposable, Contents 20/box Laryngoscope Blades. This Recall only involves lot codes Gj and Ha. This device was manufactured from July 2006 through March 2007 and distributed from January 16, 2007 through April 13, 2007.The Recall is being initiated because of the possibility that a piece of the acrylic light tube that runs along the laryngoscope blade may break off during the procedure. The... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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