OT1000 Series Orthopedic Surgical Tables — Class II medical device recall Z-2248-2016
Terminated recall by Steris Corporation, reported 2016-07-27, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. STERIS has identified that the pivot pin assembly located on the table top may become loose preventing the tab
| Recall number | Z-2248-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Steris Corporation, Mentor, OH, United States |
| Recall initiated | 2016-05-23 |
| Classified | 2016-07-20 |
| Reported by FDA | 2016-07-27 |
| Terminated | 2016-08-22 |
| Distributed | 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 |
| Countries outside the US | CA, FR, KR, PA, QA, TH |
| Quantity | 148 |
Product
OT1000 Series Orthopedic Surgical Tables
Reason for recall
STERIS has identified that the pivot pin assembly located on the table top may become loose preventing the table from articulating properly.
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-2248-2016. 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.