The 5085 is a general surgical table with high patient weight capacity — Class II medical device recall Z-0196-2015
Terminated recall by Steris Corporation, reported 2014-11-19, distributed in AL, AR, AZ, CA, CO, DC, FL, GA…. The 5085 and 5085SRT stainless steel column shrouds may become damaged as a result of misalignment during extr
| Recall number | Z-0196-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Steris Corporation, Mentor, OH, United States |
| Recall initiated | 2014-10-10 |
| Classified | 2014-11-07 |
| Reported by FDA | 2014-11-19 |
| Terminated | 2015-06-26 |
| Distributed | AL, AR, AZ, CA, CO, DC, FL, GA, HI, IA, ID, IL, IN, KY, LA, MD, ME, MI, MN, MO, MS, NC, ND, NV, NY, OH, OK, OR, RI, SC, SD, TN, TX, VA, WI, WV |
| Countries outside the US | BR, CA, CN, EC, IN, KR, MX, TH |
| Quantity | 999 |
Product
The 5085 is a general surgical table with high patient weight capacity, extended width capability, and lower minimal table top elevation.
Reason for recall
The 5085 and 5085SRT stainless steel column shrouds may become damaged as a result of misalignment during extreme table articulation, excessive side force on the table column, or pressure on the base of the table. Severe damage to the shrouds may prevent the user from raising or lowering the surgical table.
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-0196-2015. 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.