Urgent Field Safety Notice Issued for KYPHON® Directional Bone Filler (Medtronic)

June 29, 2017 A recall has been issued for all lot numbers of KYPHON® Directional Bone Void Filler, Product # F04C. The reason for this action is that it has been found that the directional arrow at the proximal end of the instrument might not correctly align with the cut‐out opening on the distal end of the instrument, which can result in serious consequences for the patient. For more information please go to (Documentation).

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