Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
KEY SAFETY SYSTEMS

KEY SAFETY SYSTEMS Recalls

All product recalls associated with KEY SAFETY SYSTEMS.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1821–1840 of 37661 recalls

Curtain Airbag Inflator (Key Safety Systems) – Ignition Holder Issue (2025)

Key Safety Systems, Inc. - (DBA Joyson) is recalling one side curtain air bag, part number 2009086-3. The ignition holder in the side curtain air bag may detach during air bag deployment.

High

NHTSAFeb 24, 2025Nationwide• KEY SAFETY SYSTEMS

COR Disposable Kit (DePuy Mitek) – Missing Pin (2025)

Device is missing the pin in the graft loader component.

Moderate

FDAFeb 24, 2025Nationwide• DePuy Mitek, Inc., a Johnson & Johnson Co.

Medline Convenience Kits (Medline) – Tube Recall Issue (2025)

Specific Medline Kits were manufactured using Intubation ORAL/NASAL Endotracheal Tubes which were subsequently recalled by Smiths Medical.

Moderate

FDA

1...90 919293 94...1884

Page 92 of 1884Next

Feb 24, 2025

• MEDLINE INDUSTRIES, LP Northfield

Livalo 4mg (Kowa) – Foreign Tablets (2025)

Presence of foreign tablets/capsules

Class IIILow

FDAFeb 24, 2025OH, PA, TX• Kowa Pharmaceuticals America

Medline Procedure Kits (Medline) – Cannula Concern (2025)

Medline medical procedure kits, containing Medtronic Aortic Root Cannula

Moderate

FDAFeb 21, 2025CA, FL, MN +6 more• MEDLINE INDUSTRIES, LP Northfield

Medline Procedure Kits (Medline) – Male Luer Material Issue (2025)

Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.

Moderate

FDAFeb 21, 2025CA, FL, MN +6 more• MEDLINE INDUSTRIES, LP Northfield

Forest River Starcraft Allstar (Forest River Bus) – Emergency Exit Issue (2025)

Forest River Bus, LLC (Forest River Bus) is recalling certain 2024 Starcraft Allstar Transit buses. The handle for the emergency exit window may not be visible to someone standing in the aisle, which can delay passengers from exiting in the event of an emergency.

Moderate

NHTSAFeb 21, 2025Nationwide• FOREST RIVER BUS

Keystone Outback (Keystone) – Window Labeling Error (2025)

Keystone RV Company (Keystone) is recalling certain 2024-2025 Outback 330RL travel trailers. The side window was incorrectly labeled as an emergency exit, which can delay passengers from exiting in the event of an emergency.

Moderate

NHTSAFeb 21, 2025Nationwide• KEYSTONE

Swagtron SG-5 Swagger 5 Electric Scooter – Battery Safety (2025)

Fire/Burn Risk

This recall involves SG-5 Swagger 5 Boost Commuter Electric Scooters sold at Walmart and Sam's Club. The electric scooters are powered by lithium-ion batteries. They were sold in black or silver colors. "SWAGGER 5" is printed in large lettering on the stem of the handlebars. The lithium-ion battery is located beneath the scooter deck. The model numbers are SWGR5-V2-SLV, SWGR5-V2-2, SG5 Boost, SG-5S, 96262-2, 96262-9, SG-5S, and 96560-2. The model numbers are affixed to the side of the scooter deck. Note: Recalled lithium-ion batteries should be disposed of in accordance with any local and state ordinances, following the procedures established by your municipal recycling center for damaged/defective/recalled lithium batteries, because these potentially hazardous batteries must be handled differently than other batteries. Do not throw this recalled battery in the trash. Do not deposit this recalled battery in used battery recycling boxes found at various retail and home improvement stores. The manufacturer, Swagtron, of South Bend, Indiana, has not been responsive to CPSC's request for information about this product or to CPSC's request for a recall. However, Walmart as the retailer has agreed to recall electric scooters that were purchased at Walmart or Sam's Club either at its stores or on its websites.

Very High

CPSCFeb 20, 2025Nationwide• Swagtron, of South Bend, Indiana

DR Field and Brush Mower – Laceration Risk (2025)

Laceration Risk

This recall involves DR Power Tow Behind Field and Brush Mowers. The black and orange tow behind mowers have the following model and serial numbers, printed on a white label that is on the front frame of the mower. "DR" is printed on the front of the mowers. Only mowers manufactured between April 1, 2024, and August 20, 2024, are included in this recall. The manufacture date is on the serial number label affixed to the rear frame of the unit and is listed in YYYYMMDD format. Model Description Serial No. Range TB21044BEN DR BRUSH MOWER PREMIER 44T 10.5 HP BS ES 3014835626 to 3015507481 TB23244BEN DR BRUSH MOWER PRO 44T 17.5 HP BS ES 3014860338 to 3015403241 TB25344BEN DR BRUSH MOWER PRO XL44T 20 HP BS ES 3014916847 to 3015451110 TB27052BEN DR BRUSH MOWER PRO MAX52T 22 HP BS ES 3014839204 to 3015534243

High

CPSCFeb 20, 2025Nationwide• DR Power Equipment, of South Burlington, Vermont, a subsidiary of Generac Power Systems Inc., of Waukesha, Wisconsin

Homebox Blackout Roller Shades – Strangulation Hazard (2025)

This recall involves Homebox Blackout Roller Window Shades with metal cords hanging from the right side. The roller blinds were sold in multiple colors including black, white and sage with sizes ranging from a width of 10-70 inches and height of 64-72 inches. "Homebox" is printed on the label sticker on the headrail.

Very High

CPSCFeb 20, 2025Nationwide• Zhejiang Mingjing Textile Co. Ltd, of China

Phenylephrine Sodium Chloride (Central Admixture) – Particulate Matter (2025)

Presence of Particulate Matter

Class IHigh

FDAFeb 20, 2025Nationwide• Central Admixture Pharmacy Services, Inc.

Centricity Universal Viewer (GE Healthcare) – Security Vulnerability (2025)

There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.

Moderate

FDAFeb 19, 2025Nationwide• GE Healthcare

Centricity Radiology RA600 (GE Healthcare) – Security Vulnerability (2025)

Moderate

FDAFeb 19, 2025Nationwide• GE Healthcare

MIM Radiological Software (MIM Software) – Image Fusion Error (2025)

In situations where two images with differing Fields of View (FOV) complete an image fusion, an incorrect, elevated Maximum Standardized Uptake Value (SUV) within MIM Software versions 7.2.0 through 7.2.6.could result.

Moderate

FDAFeb 19, 2025Nationwide• MIM Software Inc

VERICIS Merge Cardio (Merge Healthcare) – Measurement Workflow Risk (2025)

When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.

Moderate

FDAFeb 19, 2025Nationwide• Merge Healthcare, Inc.

Lazervida Laser Engraver (Flux Technology) – Performance Standards (2025)

Lazervida 10W Diode Laser Engraver does not fully meet current Federal performance standards in certain areas. Specifically, the product does not incorporate the additional beam attenuator, remote interlock connector, key switch, specific labels and manual instructions required under current regulations.

Moderate

FDAFeb 19, 2025Nationwide• Flux Technology Inc.

Stay Informed

KEY SAFETY SYSTEMS Recalls

Recall Summary

Curtain Airbag Inflator (Key Safety Systems) – Ignition Holder Issue (2025)

COR Disposable Kit (DePuy Mitek) – Missing Pin (2025)

Medline Convenience Kits (Medline) – Tube Recall Issue (2025)

Livalo 4mg (Kowa) – Foreign Tablets (2025)

Medline Procedure Kits (Medline) – Cannula Concern (2025)

Medline Procedure Kits (Medline) – Male Luer Material Issue (2025)

Forest River Starcraft Allstar (Forest River Bus) – Emergency Exit Issue (2025)

Keystone Outback (Keystone) – Window Labeling Error (2025)

Swagtron SG-5 Swagger 5 Electric Scooter – Battery Safety (2025)

DR Field and Brush Mower – Laceration Risk (2025)

Homebox Blackout Roller Shades – Strangulation Hazard (2025)

Phenylephrine Sodium Chloride (Central Admixture) – Particulate Matter (2025)

Centricity Universal Viewer (GE Healthcare) – Security Vulnerability (2025)

Centricity Radiology RA600 (GE Healthcare) – Security Vulnerability (2025)

MIM Radiological Software (MIM Software) – Image Fusion Error (2025)

VERICIS Merge Cardio (Merge Healthcare) – Measurement Workflow Risk (2025)

Centricity Cardiology CA1000 (GE Healthcare) – Security Vulnerability (2025)

Centricity PACS-IW (GE Healthcare) – Security Vulnerability (2025)

Centricity PACS-IW (GE Healthcare) – Security Vulnerability (2025)

Lazervida Laser Engraver (Flux Technology) – Performance Standards (2025)