Product Wiki · Recalls · U.S. FDA — Device Enforcement

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 Operating Table General Purpose Surgical Table

U.S. FDA — Device Enforcement · United States · 2016-04-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1844-2016
Date of alert
2016-04-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Skytron, Div. The KMW Group, Inc
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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