FDA Device recall Z-0196-2015
The 5085 is a general surgical table with high patient weight capacity, extended width capability, and lower minimal table top elevation
- FDA Device
- Class II
- terminated
- Published 2014-11-19
On 2014-11-19 the FDA classified a Class II recall of The 5085 is a general surgical table with high patient weight capacity, extended width capability, and lower minimal table top elevation by Steris, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0196-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-10-10 |
| Published | 2014-11-19 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Steris |
| Distribution | 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 |
Product
The 5085 is a general surgical table with high patient weight capacity, extended width capability, and lower minimal table top elevation.
Reason
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.
Identifiers
| code_info | 5085 and 5085SRT |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0196-2015%22
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