Skytron, Div. The KMW Group, Inc: Medical Device Recall in 2016 - (Recall #: Z-1844-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

EZ Slide Battery/line powered hydraulic table with removable leg section and 21 top slide General Purpose Surgical Table Skytron EZ Slide Operating Table General Purpose Surgical Table

Product Classification:

Class II

Date Initiated: April 6, 2016

Date Posted: June 8, 2016

Recall Number: Z-1844-2016

Event ID: 74128

Reason for Recall:

The potential exists within the identified tables that incorrectly manufactured parts have been used in assembly. If a table is found to have these incorrectly manufactured parts, it is possible for the tables elevation column slide cap to become detached from the elevation column and could result in the loss of control of the table top and injury to the patient or staff.

Status: Terminated

Product Quantity: 458

Code Information:

Model number 3502. All units. Units entered commercial distribution between April 30, 2014 and July 24, 2014

Distribution Pattern:

Nationwide Distribution to AL, AZ, CO, IA, WI, PA, TN, MA, TX, MI, FL, MS, LA, and CA.

Voluntary or Mandated:

Voluntary: Firm initiated