Steris Corporation: Medical Device Recall in 2014 - (Recall #: Z-0196-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

The 5085 is a general surgical table with high patient weight capacity, extended width capability, and lower minimal table top elevation.

Product Classification:

Class II

Date Initiated: October 10, 2014

Date Posted: November 19, 2014

Recall Number: Z-0196-2015

Event ID: 69472

Reason for Recall:

The 5085 and 5085SRT stainless steel column shrouds may become damaged as a result of misalignment during extreme table articulation, excessive side force on the table column, or pressure on the base of the table. Severe damage to the shrouds may prevent the user from raising or lowering the surgical table.

Status: Terminated

Product Quantity: 999

Code Information:

5085 and 5085SRT

Distribution Pattern:

US distribution: AL, AZ, AR, CA, CO, CN, DC, FL, GA, HI, ID, IL, IN, IA, KN, KY, LA, ME, MD, MI, MN, MS, MO, NB, NV, NY, NC, ND, OH, OK, OR, PN, RI, SC, SD, TN, TX, VA, WV, WI. Foriegn: Austrialia, Brazil, Canada, China, Ecuador, India, Korea, Mexico, Pnama, and Thailand.

Voluntary or Mandated:

Voluntary: Firm initiated