FDAMay 23, 2016device

OT1000 Series Orthopedic Surgical Tables

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

The hazard

STERIS has identified that the pivot pin assembly located on the table top may become loose preventing the table from articulating properly.

What to do

FDA enforcement status: Terminated

Brands named

steris

Recall history

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

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