Precise Treatment Table — Class II medical device recall Z-1072-2013
Terminated recall by Elekta, Inc., reported 2013-04-17, distributed nationwide. The Column rotation can accidentally be moved to a different position which in the locked position.
| Recall number | Z-1072-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Elekta, Inc., Atlanta, GA, United States |
| Recall initiated | 2013-03-14 |
| Classified | 2013-04-09 |
| Reported by FDA | 2013-04-17 |
| Terminated | 2015-03-17 |
| Distributed | Nationwide (US) |
| Quantity | 443 |
Product
Precise Treatment Table. To be used as part of radiation therapy treatment process.
Reason for recall
The Column rotation can accidentally be moved to a different position which in the locked position.
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-1072-2013. 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.