The STERIS 4085 General Surgical Table Product Usage: is an… — Class II medical device recall Z-2026-2014
Terminated recall by Steris Corporation, reported 2014-07-16, distributed nationwide. STERIS engineering analysis has determined the D1 pressure switch in the hydraulic column manifold does not ad
| Recall number | Z-2026-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Steris Corporation, Mentor, OH, United States |
| Recall initiated | 2014-06-27 |
| Classified | 2014-07-09 |
| Reported by FDA | 2014-07-16 |
| Terminated | 2015-09-16 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BR, CA, CN, CR, HK, ID, IN, KR, MX, NP, NZ, SG, SV, TW, VN |
| Quantity | 3,689 |
Product
The STERIS 4085 General Surgical Table Product Usage: is an electro-hydraulically operated surgical table designed to support all general surgical procedures.
Reason for recall
STERIS engineering analysis has determined the D1 pressure switch in the hydraulic column manifold does not adequately detect pressure level. If one or more of the table floor lock feet become unlocked due to the loss of hydraulic pressure, there is a potential for the table hand control to incorrectly indicate that the floor lock feet are locked.
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-2026-2014. 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.