Recall Z-1844-2016— Skytron, Div. The KMW Group, Inc
Class II · Terminated
Class II FDA medical device recall by Skytron, Div. The KMW Group, Inc, initiated 2016-04-06, terminated 2017-07-20. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Skytron, Div. The KMW Group, Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-04-06
- Terminated
- 2017-07-20
- Firm location
- Grand Rapids, MI, United States
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
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.