Steris Corporation recalls OT1000 Series Orthopedic Surgical Tables

Recalled July 27, 2016 · FDA recall Z-2248-2016 · Steris

Hazard

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

Units

148

Sold at

AL;AK, AZ; AR; CA; CO; CT; DC; FL; GA; IL; IN; IA; NY; NJ; NC; OH; OK; OR; PA; PR; SC; TX; UT and VA. Foreign accounts: Canada; France; Korea; Panama; Qatar and Thailand.

Description

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

Product

OT1000 Series Orthopedic Surgical Tables

Manufacturer(s)

Steris Corporation

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →