Recall Z-1266-2018— Deerfield Imaging, Inc.

Name: FDA recall Z-1266-2018
Creator: U.S. Food and Drug Administration
Published: 2018-02-23

Class II · Terminated

Class II FDA medical device recall by Deerfield Imaging, Inc., initiated 2018-02-23, terminated 2019-09-12. FDA's recall record names no specific 510(k) clearance for this event. Product: IMRIS ORT300, Removable Operating Room Table, Part Numbers: (a) 114093-000 (b) 114093-600. Reason: The Operating Room Table may drift while in use, which could potentially result in unintended movement of the table..

Recalling firm: Deerfield Imaging, Inc.
Classification: Class II
Status: Terminated
Initiated: 2018-02-23
Terminated: 2019-09-12
Firm location: Minnetonka, MN, United States

Product description

IMRIS ORT300, Removable Operating Room Table, Part Numbers: (a) 114093-000 (b) 114093-600

Reason for recall

The Operating Room Table may drift while in use, which could potentially result in unintended movement of the table.

Data sourced from openFDA. This site is unofficial and independent of the FDA.