Recall Z-2585-2021— Deerfield Imaging, Inc.
Class II · Terminated
Class II FDA medical device recall by Deerfield Imaging, Inc., initiated 2021-08-25, terminated 2024-04-30. FDA's recall record names no specific 510(k) clearance for this event. Product: Operating room table - Product Usage: intended for use during diagnostic examinations, radiologic procedures or surgical procedures to support and position a patient.. Reason: ORT200/300 rotational lock may fail to function such that it cannot change states between locked and unlocked, due to a mechanical hardware issue..
- Recalling firm
- Deerfield Imaging, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2021-08-25
- Terminated
- 2024-04-30
- Firm location
- Minnetonka, MN, United States
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.