Defect in the outer packaging of the Cranial Access Kits. can cause the packaging to split without any additional forces outside compromising the sterility of the device
Reason for recall: Defect in the outer packaging of the Cranial Access Kits. can cause the packaging to split without any additional forces outside compromising the sterility of the device Distribution: Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Belgium, Canada, Chile, France, Ireland, Israel, South Africa, United Kingdom. Quantity: 510 units Lot/code info: UDI-DI: 10381780431923 Lot Number/Exp. Date: 6561324 1-Aug-24 6844177 1-Mar-25 7078242 1-May-25
10381780431923
Official record: FDA (Device enforcement) ↗
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