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Medtronic Infuse Bone Graft OR RHBMP2
No active recall
Manufacturer: Medtronic · FDA product code: NEK · Category: Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction
Severity Snapshot
481 total reports2012-10 – 2013-11 date range0% physician / facility reported0% manufacturer reported1 SKU variants
Failure & Consequence Profiles
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Reporting Trend
Annual Reporting Volume
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Note: the 2018 Voluntary Malfunction Summary Reporting expansion means volume increases may reflect surveillance changes, not increased device risk.
Reported Events
Submitted to FDA MAUDE by physicians, hospitals, manufacturers, and patients.
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