Class II FDA device recall · Z-2469-2023

Class II — the FDA judged the product may cause temporary or medically reversible harm, with a remote chance of serious harm.

This is the FDA's risk judgment for this recall. It describes the potential of the product as a category — it does not establish that any specific unit harmed anyone. Most recalls are Class II or III.

GS70 Salus Surgical Table, Product Code 18-070-70

Why it was recalled

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.

Is your unit affected?

The recall covers only the specific lots or serial numbers the FDA listed. Enter the lot or serial number from your product's label and we'll check it against that list.

A match means your unit may be covered — stop and call your pharmacist before doing anything. No match suggests it isn't covered, but confirm anyway: code formats vary and lists can be incomplete. Your unit not being listed does not guarantee it is safe, and being listed does not mean you have been harmed.

Show the FDA's listed lot / 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

Recall status

Ongoing — the recall is still being carried out.

Where it was distributed

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.

Recall record

Recalling firm: Skytron, LLC
Product type: Devices
Recall number: Z-2469-2023
Voluntary / mandated: Voluntary: Firm initiated
Initial notification: Letter
Origin: Grand Rapids, MI
Recall initiated: 2023-08-01

What to do

Check the lot/code above against your product. To confirm this record and read the FDA's full notice, see the FDA recall page. Before changing anything you take or use, ask your pharmacist or prescriber — this page does not tell you to start or stop any drug or device.

Also available: structured data (JSON-LD) · recall record (JSON)

What this is — and is not

A recall is a recorded FDA enforcement action — the FDA logged that a firm is removing or correcting a product. It does not establish that any specific unit harmed anyone, and causation is not established by a recall. The class above is the FDA's risk judgment for the product category, not a finding about your unit. This page informs and compares; it is not medical advice and never tells you to start or stop a drug or device.

To report a problem you experienced, use FDA MedWatch. Verify this record at FDA recalls · Recall Z-2469-2023 · Source: openFDA enforcement.