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Clariance Recalls

1 recall on record · July 24, 2019 to July 24, 2019 · Medical Devices

July 24, 2019Medical DevicesFDA

Clariance Inc recalls Erisma- LP posterior fixation system with the below specifically affected products: 1. Erisma-LP polyaxial screws -

Hazard: Potential for the polyaxial screw to become disassembled during implant.

Clariance Recalls | RecallWatchUSA