FDA Device recall Z-1149-2021
OT1000 Series Orthopedic Surgical Tables
- FDA Device
- Class II
- terminated
- Published 2021-03-03
On 2021-03-03 the FDA classified a Class II recall of OT1000 Series Orthopedic Surgical Tables by Steris, citing 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 t….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1149-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-01-21 |
| Published | 2021-03-03 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Steris |
| Distribution | 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 |
Product
OT1000 Series Orthopedic Surgical Tables
Reason
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.
Identifiers
| code_info | Model No.: OT1000, OT1100, OT1200 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1149-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.