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U.S. Department of Health and Human Services

Class 2 Device Recall GS70 Salus

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  Class 2 Device Recall GS70 Salus see related information
Date Initiated by Firm August 01, 2023
Date Posted August 28, 2023
Recall Status1 Open3, Classified
Recall Number Z-2469-2023
Recall Event ID 92290
Product Classification Table, operating-room, electrical - Product Code GDC
Product GS70 Salus Surgical Table, Product Code 18-070-70
Code Information Serial Numbers: SUC-20207-0006 SUC-20208-0025 SUC-20209-0044 SUC-20212-0063 SUC-20228-0082 SUC-2022Y-0101 SUC-20207-0007 SUC-20208-0026 SUC-20209-0045 SUC-20212-0064 SUC-20228-0083 SUC-2022Y-0102 SUC-20207-0008 SUC-20208-0027 SUC-2020X-0046 SUC-20212-0065 SUC-20228-0084 SUC-2022Y-0103 SUC-20207-0009 SUC-20208-0028 SUC-2020X-0047 SUC-20226-0066 SUC-20228-0085 SUC-2022Y-0104 SUC-20207-0010 SUC-20208-0029 SUC-2020X-0048 SUC-20226-0067 SUC-20228-0086 SUC-2022Y-0105 SUC-20207-0011 SUC-20209-0030 SUC-2020X-0049 SUC-20226-0068 SUC-20228-0087 SUC-20231-0106 SUC-20207-0012 SUC-20209-0031 SUC-2020X-0050 SUC-20226-0069 SUC-20228-0088 SUC-20231-0107 SUC-20207-0013 SUC-20209-0032 SUC-2020X-0051 SUC-20226-0070 SUC-20228-0089 SUC-20231-0108 SUC-20208-0014 SUC-20209-0033 SUC-2020X-0052 SUC-20227-0071 SUC-20228-0090 SUC-20231-0109 SUC-20208-0015 SUC-20209-0034 SUC-2020X-0053 SUC-20227-0072 SUC-20229-0091 SUC-20231-0110 SUC-20208-0016 SUC-20209-0035 SUC-2020X-0054 SUC-20227-0073 SUC-20229-0092 SUC-20231-0111 SUC-20208-0017 SUC-20209-0036 SUC-2020X-0055 SUC-20227-0074 SUC-20229-0093 SUC-20231-0112 SUC-20208-0018 SUC-20209-0037 SUC-2020Y-0056 SUC-20227-0075 SUC-20229-0094 SUC-20231-0113 SUC-20208-0019 SUC-20209-0038 SUC-2020Y-0057 SUC-20228-0076 SUC-20229-0095 SUC-20231-0114 SUC-20208-0020 SUC-20209-0039 SUC-2020Y-0058 SUC-20228-0077 SUC-2022X-0096 SUC-20231-0115 SUC-20208-0021 SUC-20209-0040 SUC-2020Y-0059 SUC-20228-0078 SUC-2022X-0097 SUC-20208-0022 SUC-20209-0041 SUC-2020Y-0060 SUC-20228-0079 SUC-2022X-0098 SUC-20208-0023 SUC-20209-0042 SUC-20212-0061 SUC-20228-0080 SUC-2022X-0099 SUC-20208-0024 SUC-20209-0043 SUC-20212-0062 SUC-20228-0081 SUC-2022X-0100
Recalling Firm/
Skytron, LLC
5085 Corporate Exchange Blvd SE
Grand Rapids MI 49512-5515
For Additional Information Contact
Manufacturer Reason
for Recall
When the control of the operating table was used in Bluetooth mode, the operating table continued moving even after releasing the button on the control. Originally, the root cause was thought to be confined to Bluetooth/wireless communications between the control pendant and the surgical table. However, during investigation, Mizuho discovered that the failure could be replicated even in wired mode if communication between the pendant and table were somehow interrupted. The root cause appears to be: if communication between the controller and table is interrupted while a button is pressed, the table does not know if/when a button is released. This occurs in wireless or wired mode.
FDA Determined
Cause 2
Under Investigation by firm
Action An URGENT: Medical Device Correction dated 7/25/23 was sent to customers. Actions to be taken by the user: 1. Please promptly forward this notification if the device has been transferred to any other entity. 2. Please review appendices of affected serial and UDI numbers and identify devices within your facility. 3. Please do not use the table control in Bluetooth mode until the correction has been installed. 4. Please contact quality at quality@skytron.com with any questions. Skytron authorized service technicians will contact affected facilities to schedule this service. A location with a medical outlet and a power cord for the operating table available will be required to complete the corrective action. Skytron estimates that this correction activity will be completed by December 31, 2023. Please do not use the table control in Bluetooth mode until the correction has been installed.
Quantity in Commerce 110 units
Distribution Worldwide - US Nationwide distribution in the states of AL, AR, CA, CT, FL, GA, IA, IL, IN, MA, MI, MO, PA, TN, TX, UT, WA, WI and the countries of Australia, New Zealand.
Total Product Life Cycle TPLC Device Report

1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.