Steris Corp Cmax 110v Surgical Table Hand Control. The Cmax Surgical Table is a mobile, electro-hydraulically operated surgical table designed to support all general surgical procedures, with the addition of STERIS table accessories. Tabletop positioning and articulations are controlled via the hand control. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Cmax 110v Surgical Table Hand Control. The Cmax Surgical Table is a mobile, electro-hydraulically operated surgical table designed to support all general surgical procedures, with the addition of STERIS table accessories. Tabletop positioning and articulations are controlled via the hand control.
Brand
Steris Corp
Lot Codes / Batch Numbers
Model Number(s): 2182625, Serial Numbers: AC0001 to AC0221.
Products Sold
Model Number(s): 2182625; Serial Numbers: AC0001 to AC0221.
Steris Corp is recalling Cmax 110v Surgical Table Hand Control. The Cmax Surgical Table is a mobile, electro-hydraulically o due to A limited quantity of the Cmax Hand Controls, P150832-500, were manufactured without Loctite thread locker on the screws that attach the mounting clip. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
A limited quantity of the Cmax Hand Controls, P150832-500, were manufactured without Loctite thread locker on the screws that attach the mounting clip to the hand control case. This clip provides a means of storing the hand control on the table side rails. It is possible that screws without Loctite can work loose and the clip can become separated from the hand control. If both screws back out c
Recommended Action
Per FDA guidance
Steris Corp. issued an "Urgent Product Correction" notice dated May 12, 2009 informing consignees of the affected device and that a Steris Service Representative with be in contact to make the necessary inspection and repairs to the device. Steris Field Service Dispatch can be reached at 1-800-288-2805. For further questions, contact Steris at 1-800-548-4873 extension 27318.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AR, CA, CO, FL, GA, HI, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MO, NE, NV, NH, NM, NY, NC, ND, OH, OR, PA, RI, SC, TN, TX, UT, VA, WV, WI
Page updated: Jan 10, 2026