FDA Device recall Z-1488-2013
Hand Controls for Operon D750, D752, D760, D820 and D850 The hand controls are used to operate OPERON surgical tables
- FDA Device
- Class II
- terminated
- Published 2013-06-12
On 2013-06-12 the FDA classified a Class II recall of Hand Controls for Operon D750, D752, D760, D820 and D850 The hand controls are used to operate OPERON surgical tables by Berchtold, citing the firm received complaints for unintended movements.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1488-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-03-12 |
| Published | 2013-06-12 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Berchtold |
| Distribution | US |
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.
Identifiers
| code_info | The hand controls are neither serialized nor lot coded. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1488-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.