| Subject: | FDA Announced Recall of Cordis CROSSOVER Sheath Introducer |
| Category: | Food and Drug Administration (FDA)
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| Published: | Mon, 2 Nov 2009 - 01:00 pm |
| Audience: Interventional radiological healthcare professionals, hospital risk managersThe Food and Drug Administration (FDA) and Cordis have notified healthcare professionals of a nationwide recall of all lots of the CROSSOVER Sheath Introducer, a long-coil reinforced, kink-resistant catheter sheath intended for use in arterial and venous procedures requiring the percutaneous introduction of therapeutic or diagnostic intravascular devices or fluids. The recall was due to stretching or fracture... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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