The recall includes the following models within the specified serial number ranges:
- GlideScope GVL 3, 0574-0007: MD10500 to MD112387
- GlideScope GVL 4, 0574-0001: LG105000 to LG112758
- GlideScope GVL 5, 0574-0030: XL105000 to XL111798
The recalled blades were manufactured between December 2010 and August 2011. They have been found to be prone to developing cracks and/or breaking across the tip of the blade.
Related Articles on Recalls:
FDA Issues Recall of Mindray Anesthesia Delivery System
DA Issues Class I Recall for Select HeartSine Public-Access Defibrillators
Mindray Anesthesia Delivery System Voluntarily Recalled
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