Skytron, Div. The KMW Group, Inc: FDA recalls

FDA enforcement reports name Skytron, Div. The KMW Group, Inc as the recalling firm in 9 events. The events have 9 product records. The recalls started from 2015 to 2022. All the events are device recalls.

See the 9 events

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on 1 Oct 2026. openFDA export of 28 Sep 2026.

Enforcement events

9 events, newest first.

FDA enforcement events of Skytron, Div. The KMW Group, Inc
Initiated	Product (first record)	Type	Class	Records	Status
2 Jun 2022	Product Name: GCX Channel Mounting Accessory Model/Catalog Number: H8-300-40-A	Device	Class II	1	Ongoing
11 May 2021	Skyton Bracket Flatscreen, Revision 2 & 3-The FS32 is a single monitor mounting bracket intended for use with a 32 inch (maximum) flat screen monitor. Model: FS32	Device	Class II	1	Ongoing
11 Sep 2020	VGDF-SKY (R4-010-06) VGA TO FIBER CONVERTER-Single Format Faceplate, a component of the SkyVision Linx 300 Integration Control System Model: VGDF-SKY (version 2). For communication and visual image management in the operating room suite.	Device	Class II	1	Terminated
10 Mar 2020	SkyVision SDS System - Video Integration Model: GC-SDS-BSCB-200 - Product Usage: is a high quality, self-contained video switching and control unit for use in the operating room.	Device	Class II	1	Terminated
5 Mar 2020	Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket, single monitor mount, 27" max. screen size Part number 3FCM1	Device	Class II	1	Ongoing
18 Apr 2019	Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam Product Usage: The SKYTRON Integrity 270 Steam Sterilizer for use in health care facilities. The Integrity Sterilizer incorporates high-pressure steam to sterilize nonporous or porous items and materials used in the health care industry	Device	Class II	1	Terminated
6 Apr 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	Device	Class II	1	Terminated
28 Mar 2016	Ergon III Series Skyboom Monitor Bracket. Part # 3FCM1 Flatscreen Bracket, single monitor mount, 27inch max. screen size	Device	Class II	1	Terminated
2 Dec 2015	Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for display interfaces utilized in clinical applications for viewing purposes and to provide an articulating point of movement on the ceiling mounted radial arm suspension system of the Ergon 2 equipment pendant / booms	Device	Class II	1	Terminated

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

Follow by RSS:Food, drug and device recallsFDA Class I recalls

Type and class

Skytron, Div. The KMW Group, Inc: events for each product type
Type		Events
Device		9

Skytron, Div. The KMW Group, Inc: events in each class
Class		Events
Class II		9

Share of the events of the firm in Class I: 0%
Share of all events on the register in Class I: 18%
Events with the status Ongoing: 3

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of Skytron, Div. The KMW Group, Inc, by the year that the recall started. The largest year is 2020, with 3 events.

Official channels

FDA enforcement reportsThe FDA search of the weekly enforcement reports.
FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
FDA: report a problemThe FDA page that shows where a report about a product goes.
FDA MedWatchThe FDA safety reporting program for drugs and medical devices.

Cite this page

Recall Register. Skytron, Div. The KMW Group, Inc: FDA recalls. https://recallregister.com/firm/skytron-div-the-kmw-group-inc/. Source: openFDA enforcement reports. Data through 28 Sep 2026.

Sources

Source: openFDA enforcement reports
Licence: CC0 1.0
Export date: 28 Sep 2026
State of the firm address: MI

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of Skytron, Div. The KMW Group, Inc have?: Class II: 9 events. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of Skytron, Div. The KMW Group, Inc?: FDA event 90400, which the firm started on 2 Jun 2022. The first product in the record is: Product Name: GCX Channel Mounting Accessory Model/Catalog Number: H8-300-40-A
How many FDA recalls of Skytron, Div. The KMW Group, Inc have the status Ongoing?: 3 events have the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.