# FDA recall Z-1149-2021

> **Steris Corporation** · Class II · device recall initiated 2021-01-21.

## 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.

## Distribution

Domestic: AL, AK, AR, AZ, CA, CO, CT, DC, FL, GA, ID, IL IN, IW, KS, KY, LA, ME, MD, MI, MN, MO, NE, NV, NJ, NY, NC, ND, OH, OK, OR, PA, PR, SC, TX, UT, VT, VA, WA, WV, WI. Foreign: Canada, South Korea, Panama, Qatar, Thailand.

## Key facts

- **Recall number:** Z-1149-2021
- **Recalling firm:** Steris Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-01-21
- **Report date:** 2021-03-03
- **Termination date:** 2021-11-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mentor, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1149-2021

## Citation

> AI Analytics. FDA recall Z-1149-2021. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1149-2021. Source: US FDA. Licensed CC0.

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