Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

OT1000 Series Orthopedic Surgical Tables Recalled by Steris Corporation Due to STERIS has identified that the pivot pin assembly...

Date: May 23, 2016
Company: Steris Corporation
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Steris Corporation directly.

Affected Products

OT1000 Series Orthopedic Surgical Tables

Quantity: 148

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed to 24 states: AL, AK, AZ, AR, CA, CO, CT, FL, GA, IL, IN, IA, NJ, NY, NC, OH, OK, OR, PA, SC, TX, UT, VA, DC

Affected (24 states)Not affected

About Steris Corporation

Steris Corporation has 109 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report