PlainRecalls
FDA Devices Moderate Class II Terminated

Operating room table - Product Usage: intended for use during diagnostic examinations, radiologic procedures or surgical procedures to support and position a patient.

Reported: October 6, 2021 Initiated: August 25, 2021 #Z-2585-2021

Product Description

Operating room table - Product Usage: intended for use during diagnostic examinations, radiologic procedures or surgical procedures to support and position a patient.

Reason for Recall

ORT200/300 rotational lock may fail to function such that it cannot change states between locked and unlocked, due to a mechanical hardware issue.

Details

Recalling Firm
Deerfield Imaging, Inc.
Units Affected
10 units
Distribution
Worldwide distribution - US Nationwide distribution FL, NH, TX, OH, CA, OR, UT, TN, NC and the countries of Canada, Australia, Sweden, Japan.
Location
Minnetonka, MN

Frequently Asked Questions

What product was recalled?
Operating room table - Product Usage: intended for use during diagnostic examinations, radiologic procedures or surgical procedures to support and position a patient.. Recalled by Deerfield Imaging, Inc.. Units affected: 10 units.
Why was this product recalled?
ORT200/300 rotational lock may fail to function such that it cannot change states between locked and unlocked, due to a mechanical hardware issue.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 6, 2021. Severity: Moderate. Recall number: Z-2585-2021.