Recall Z-1488-2013— Berchtold Corp.
Class II · Terminated
Class II FDA medical device recall by Berchtold Corp., initiated 2013-03-12, terminated 2017-05-08. FDA's recall record names no specific 510(k) clearance for this event. Product: Hand Controls for Operon D750, D752, D760, D820 and D850 The hand controls are used to operate OPERON surgical tables. Reason: The firm received complaints for unintended movements..
- Recalling firm
- Berchtold Corp.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2013-03-12
- Terminated
- 2017-05-08
- Firm location
- N Charleston, SC, United States
Product description
Hand Controls for Operon D750, D752, D760, D820 and D850 The hand controls are used to operate OPERON surgical tables
Reason for recall
The firm received complaints for unintended movements.
Data sourced from openFDA. This site is unofficial and independent of the FDA.