RecallRadar

FDA Device recall Z-2402-2012

A mobile, electro-hydraulically operated, fluoroscopic/C-Arm compatible general surgical table

On 2012-09-26 the FDA classified a Class II recall of A mobile, electro-hydraulically operated, fluoroscopic/C-Arm compatible general surgical table by Steris, citing customers may be storing objects on the base and/or around the column of the surgical table. This prohibited practice and misuse known by the customers can damage the override swi….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2402-2012
ClassificationClass II
Statusterminated
Initiated2010-02-17
Published2012-09-26
Last updated2026-09-13 11:53 UTC
CompanySteris
DistributionUS

Product

A mobile, electro-hydraulically operated, fluoroscopic/C-Arm compatible general surgical table. Product Usage: Product provides a flexible, easy-to-use, articulated posturing of a patient for either general, I.A., or specialized surgical procedures. There are movable components and accessories intended for use during diagnostic examinations or surgical procedures to support and position a patient.

Reason

Customers may be storing objects on the base and/or around the column of the surgical table. This prohibited practice and misuse known by the customers can damage the override switch assembly located at the top of the column cover. Depending upon the nature and severity of the damage to the electronics of the table, it is possible that the table could move without prompting by an operator .

Identifiers

code_infoB420702032 to 0402110097

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2402-2012%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.