| Subject: | Class I Recall of Stryker Custom Cranial Implant Kits |
| Category: | Food and Drug Administration (FDA)
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| Published: | Fri, 26 Dec 2008 - 01:00 pm |
| Audience: Maxillofacial surgeons, hospital risk managers Stryker Leibinger USA and the FDA have notified healthcare professionals of a Class I Recall of all sizes of the cranial implant kit distributed from November 5, 2007 through October 23, 2008. The company is recalling these products because sterility cannot be assured. Custom cranial implants are designed individually for each patient to correct trauma and/or defects in the lower jaw, upper jaw and face or the cranium and the face.... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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