FDA DeviceClass IINotable
FDA Recall: Hintermann Series Talar Implant, Left, Size 2 REF 302112
Description
Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.
Hazard
Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.
Remedy
67 units
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