Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
OT1000 Series Orthopedic Surgical Tables Recalled by Steris Corporation Due to On January 7, 2021, STERIS identified that the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Steris Corporation directly.
Affected Products
OT1000 Series Orthopedic Surgical Tables
Quantity: 272 tables total (Domestic: 227 tables, Foreign 45 tables)
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 39 states: AL, AK, AZ, AR, CA, CO, CT, FL, GA, ID, IL, IN, KS, KY, LA, ME, MD, MI, MN, MO, NE, NV, NJ, NY, NC, ND, OH, OK, OR, PA, SC, TX, UT, VT, VA, WA, WV, WI, DC
About Steris Corporation
Steris Corporation has 109 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report