Skytron, Div. The KMW Group, Inc recalls
Every recall we track for Skytron, Div. The KMW Group, Inc — 6 in all, from 2019–2022 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Skytron, Div. The KMW Group, Inc peaked in 2020 (3); 6 since 2017.
All FDA recall records for Skytron, Div. The KMW Group, Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 1 | 0 | 0 | 1 |
| 2020 | 0 | 2 | 1 | 0 | 3 |
| 2021 | 0 | 1 | 0 | 0 | 1 |
| 2022 | 0 | 1 | 0 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Skytron, Div. The KMW Group, Inc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Skytron, Div. The KMW Group, Inc recalls
6 shown- Use cautionMedical device
Skytron, Div. The KMW Group, Inc recalls Product Name: GCX Channel Mounting Accessory Model/Catalog Number: H8-300-40-A
Skytron recalls GCX Channel Mounting Accessory model H8-300-40-A due to risk of mounting screws loosening when used with VST clamp on Ergon 3 boom. Affected units lack UDI and were sold after September 2016.
SkytronJun 2, 2022 - Use cautionMedical device
Skytron, Div. The KMW Group, Inc recalls Skyton Bracket Flatscreen, Revision 2 & 3-The FS32 is a single monitor mounting bracket intended for use with a 32 inch
Recall of Skyton Bracket Flatscreen Revision 2 & 3 FS32 monitor mounting brackets due to risk of detachment causing injury to patients or staff. Serial numbers listed in updated notice.
SkytronMay 11, 2021 - Lower riskMedical device
Skytron, Div. The KMW Group, Inc recalls VGDF-SKY (R4-010-06) VGA TO FIBER CONVERTER-Single Format Faceplate, a component of the SkyVision Linx 300 Integration
Skytron recalls VGDF-SKY (R4-010-06) VGA to Fiber Converter for potential video signal failure in SkyVision Linx 300 systems. Affected units may lose video display on secondary screens.
SkytronSep 11, 2020 - Use cautionMedical device
Skytron, Div. The KMW Group, Inc recalls SkyVision SDS System - Video Integration Model: GC-SDS-BSCB-200 - Product Usage: is a high quality, self-contained
Skytron recalls 20+ operating room video systems that may cause monitor blanking during surgery, risking patient safety. Affected units have specific serial numbers.
SkytronMar 10, 2020 - Use cautionMedical device
Skytron, Div. The KMW Group, Inc recalls Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket, single monitor mount, 27" max. screen size Part
Skytron recalls Ergon 3 Series Skyboom Monitor Brackets with potential weld failure at pivot point, risking display falls and injury. Affected units have specific serial numbers.
SkytronMar 5, 2020 - Use cautionMedical device
Skytron, Div. The KMW Group, Inc recalls Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam Product Usage: The SKYTRON Integrity 270 Steam
Skytron recalls Integrity 270 Steam Sterilizers with serial numbers 14092619-18113521 due to potential weld failure in air heater assembly. This could cause equipment malfunction in healthcare settings.
SkytronApr 18, 2019
Skytron, Div. The KMW Group, Inc recall questions
How many recalls has Skytron, Div. The KMW Group, Inc had?
6 recalls from Skytron, Div. The KMW Group, Inc are on record with U.S. safety agencies, from 2019–2022.
What is the most recent Skytron, Div. The KMW Group, Inc recall?
Skytron, Div. The KMW Group, Inc recalls Product Name: GCX Channel Mounting Accessory Model/Catalog Number: H8-300-40-A, dated Jun 2, 2022. Every Skytron, Div. The KMW Group, Inc recall is listed on this page, newest first.
What should I do if I have a recalled Skytron, Div. The KMW Group, Inc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Skytron, Div. The KMW Group, Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.