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INSTRUMENT READINESS

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Results<br />

Endoscopic evaluation of Arthoscopic instruments<br />

revealed retained tissue in the lumen of the<br />

inflow/outflow cannulae and arthroscopic shaver hand<br />

piece.<br />

Changes in instrument reprocessing protocols were<br />

implemented<br />

Safety alert issued by US FDA about concern of retained<br />

tissue in arthroscopic shavers<br />

Conclusions<br />

SSI related to surgical instrument contamination with<br />

Pseudomonas during instrument reprocessing<br />

Retained tissue in inflow/outlaw cannula and shaver<br />

hand pieces could have allow bacteria to survive<br />

sterilization procedures.

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