Recall Z-2248-2016— Steris Corporation
Class II · Terminated
Class II FDA medical device recall by Steris Corporation, initiated 2016-05-23, terminated 2016-08-22. FDA's recall record names no specific 510(k) clearance for this event. Product: OT1000 Series Orthopedic Surgical Tables. Reason: STERIS has identified that the pivot pin assembly located on the table top may become loose preventing the table from articulating properly..
- Recalling firm
- Steris Corporation
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-05-23
- Terminated
- 2016-08-22
- Firm location
- Mentor, OH, United States
Product description
OT1000 Series Orthopedic Surgical Tables
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.