RecallRadar

FDA Device recall Z-1844-2016

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

On 2016-06-08 the FDA classified a Class II recall of EZ Slide Battery/line powered hydraulic table with removable leg section and 21 top slide General Purpose Surgical Table Skytron EZ Slide… by Skytron Div The Kmw Group, citing 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,….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1844-2016
ClassificationClass II
Statusterminated
Initiated2016-04-06
Published2016-06-08
Last updated2026-09-13 11:54 UTC
CompanySkytron Div The Kmw Group
DistributionUS

Product

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

Reason

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.

Identifiers

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

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1844-2016%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.