Boston Scientific Recalls OverStitch Suture Cinch Over Deployment Failure Risk
FDA classifies recall of endoscopic tissue approximation device as Class II due to potential failure to deploy cinch or cut suture.
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FDA classifies recall of endoscopic tissue approximation device as Class II due to potential failure to deploy cinch or cut suture.
Boston Scientific Corporation initiated an ongoing recall for thousands of biopsy forceps due to a potential packaging breach.
An FDA enforcement report classifies the ongoing Class II recall of more than 150,000 US units of the endoscopy injection set, citing a recalled component syringe that may loosen from the manifold.