Recall Z-2168-2013— Berchtold Corp.
Class II · Terminated
Class II FDA medical device recall by Berchtold Corp., initiated 2012-04-16, terminated 2013-09-10. FDA's recall record names no specific 510(k) clearance for this event. Product: OPERON D850 Surgical Table Product Usage: Surgical Table. Reason: Table was not lowering..
- Recalling firm
- Berchtold Corp.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2012-04-16
- Terminated
- 2013-09-10
- Firm location
- N Charleston, SC, United States
Product description
OPERON D850 Surgical Table Product Usage: Surgical Table
Reason for recall
Table was not lowering.
Data sourced from openFDA. This site is unofficial and independent of the FDA.