Skytron, Div. The KMW Group, Inc

Complete recall history across all FDA and CPSC categories — 9 total recalls

Skytron, Div. The KMW Group, Inc appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (9)

FDA medical device enforcement actions by Skytron, Div. The KMW Group, Inc

Date Product Reason Class
Jun 2, 2022 Product Name: GCX Channel Mounting Accessory Model/Catalog Number: H8-300-40-A Under certain circumstances, the mounting screws may loosen or pull out from ... Class II
May 11, 2021 Skyton Bracket Flatscreen, Revision 2 & 3-The FS32 is a single monitor mounti... Failure of the FS32 Monitor Brackets from the mounting block could potentiall... Class II
Sep 11, 2020 VGDF-SKY (R4-010-06) VGA TO FIBER CONVERTER-Single Format Faceplate, a compon... VGDF (VGA) Faceplate failure results in failure of video signal for SkyVision... Class II
Mar 10, 2020 SkyVision SDS System - Video Integration Model: GC-SDS-BSCB-200 - Product Us... Intermittent failure of a signal being sent to a monitor from the touch panel... Class II
Mar 5, 2020 Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket, single mon... Potential for the weld to fail at the pivot point of the monitor bracket. Thi... Class II
Apr 18, 2019 Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam P... Weld attaching the air heater assembly to the main sterilizer unit has shown ... Class II
Apr 6, 2016 EZ Slide Battery/line powered hydraulic table with removable leg section and ... The potential exists within the identified tables that incorrectly manufactur... Class II
Mar 28, 2016 Ergon III Series Skyboom Monitor Bracket. Part # 3FCM1 Flatscreen Bracket, s... Potential for the weld to fail at the pivot point of the monitor bracket. Th... Class II
Dec 2, 2015 Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for di... The hardware that holds the VESA plate and the display interface / monitor to... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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