Steris Corporation: Medical Device Recall in 2016 - (Recall #: Z-2248-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

OT1000 Series Orthopedic Surgical Tables

Product Classification:

Class II

Date Initiated: May 23, 2016

Date Posted: July 27, 2016

Recall Number: Z-2248-2016

Event ID: 74264

Reason for Recall:

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

Status: Terminated

Product Quantity: 148

Code Information:

OT1000, OT1100, and OT1200 Orthopedic Surgical Table

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated