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New Era Orthopaedics Recalls

1 recall on record · August 15, 2018 to August 15, 2018 · Medical Devices

August 15, 2018Medical DevicesFDA

New Era Orthopaedics, LLc recalls Modera Modular Pedicle Screw System Shank Insertion Instrument, 3-107-07

Hazard: This is a retrospective recall of an instrument used in spine fusion procedures with Modera Modular Pedicle Screw system implants. The firm received a customer complaint in which excessive forces were applied to the shank insertion instrument and the laser weld failed.

New Era Orthopaedics Recalls | RecallWatchUSA