Hand Controls for Operon D750 — Class II medical device recall Z-1488-2013
Terminated recall by Berchtold Corp., reported 2013-06-12, distributed nationwide. The firm received complaints for unintended movements.
| Recall number | Z-1488-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Berchtold Corp., N Charleston, SC, United States |
| Recall initiated | 2013-03-12 |
| Classified | 2013-06-06 |
| Reported by FDA | 2013-06-12 |
| Terminated | 2017-05-08 |
| Distributed | Nationwide (US) |
| Quantity | 3,763 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1488-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.