FDAApril 22, 2016device

Streamline OCT Occipito-Cervico-Thoracic System, Crosslink Counter Torque Sleeve. Spinal fixation device instrument.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Potential for a product defect where the cannula may be obstructed. This obstruction could prevent a driver from going through, which increases the potential for the driver to slip, resulting in possible patient injury.

What to do

FDA enforcement status: Terminated

Brands named

rti surgical inc dba pioneer surgical technology incrtirti surgical

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Streamline OCT Occipito-Cervico-Thoracic System, Crosslink Counter Torque Sleeve. Spinal fixation device instrument. — Recall Details · AllClear