OPERON D850 Surgical Table Product Usage: Surgical Table — Class II medical device recall Z-2168-2013
Terminated recall by Berchtold Corp., reported 2013-09-18, distributed nationwide. Table was not lowering.
| Recall number | Z-2168-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Berchtold Corp., N Charleston, SC, United States |
| Recall initiated | 2012-04-16 |
| Classified | 2013-09-09 |
| Reported by FDA | 2013-09-18 |
| Terminated | 2013-09-10 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 263 |
Product
OPERON D850 Surgical Table Product Usage: Surgical Table
Reason for recall
Table was not lowering.
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-2168-2013. 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.