OT1000 Series Orthopedic Surgical Tables — Class II medical device recall Z-1149-2021
Terminated recall by Steris Corporation, reported 2021-03-03, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. On January 7, 2021, STERIS identified that the glued bond between the beam and the leg spar assembly may begin
| Recall number | Z-1149-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Steris Corporation, Mentor, OH, United States |
| Recall initiated | 2021-01-21 |
| Classified | 2021-02-24 |
| Reported by FDA | 2021-03-03 |
| Terminated | 2021-11-10 |
| Distributed | AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, ID, IL, IN, KS, KY, LA, MD, ME, MI, MN, MO, NC, ND, NE, NJ, NV, NY, OH, OK, OR, PA, PR, SC, TX, UT, VA, VT, WA, WI, WV |
| Countries outside the US | CA, KR, PA, QA, TH |
| Model numbers | OT1000, OT1100, OT1200 |
Product
OT1000 Series Orthopedic Surgical Tables
Reason for recall
On January 7, 2021, STERIS identified that the glued bond between the beam and the leg spar assembly may begin to separate over time. This could result in unexpected movement of the affected leg spar if the separation occurred during a patient procedure.
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-1149-2021. 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.