Stryker Craniomaxillofacial Issues Nationwide Recall of its Custom Cranial Implant Kits; Catalogue Numbers 54-00101, 54-00102, 54-00103 and 54-00104,

Contact:
Patrick Anderson, Stryker Corporation
(269) 385-7253
Patrick.Anderson@Stryker.com
Aaron Kwittken, Kwittken & Company
(646) 747-7144

AKwittken@Kwitco.com

FOR IMMEDIATE RELEASE – Portage, Mich.,– Dec. 23, 2008 — Stryker’s Craniomaxillofacial (CMF) business unit announced today that the U.S. Food and Drug Administration (FDA) concluded on Dec. 18, 2008 that its recall of the following Stryker CMF’s Custom Cranial Implant Kits is a Class I recall, which means the product could pose an imminent hazard to health: Catalogue Numbers 54-00101, 54-00102, 54-00103 and 54-00104, all lots shipped sterile.

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