FDA Device recall Z-2248-2016
OT1000 Series Orthopedic Surgical Tables
- FDA Device
- Class II
- terminated
- Published 2016-07-27
On 2016-07-27 the FDA classified a Class II recall of OT1000 Series Orthopedic Surgical Tables by Steris, citing STERIS has identified that the pivot pin assembly located on the table top may become loose preventing the table from articulating properly.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2248-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-05-23 |
| Published | 2016-07-27 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Steris |
| Distribution | AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, IA, IL, IN, NC, NJ, NY, OH, OK, OR, PA, PR, SC, TX, UT, VA |
Product
OT1000 Series Orthopedic Surgical Tables
Reason
STERIS has identified that the pivot pin assembly located on the table top may become loose preventing the table from articulating properly.
Identifiers
| code_info | OT1000, OT1100, and OT1200 Orthopedic Surgical Table |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2248-2016%22
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