stop use immediately Recalls

Beckman Coulter Recalls 160 DxC 500i Modules and DxI 9000 Analyzers in 2025 Recall

Wuensche USA Recalls Ambiano Cotton Candy Makers 836098 Over Fire Hazard (2025)

Wuensche USA recalls Ambiano Cotton Candy Makers, model 836098, sold at ALDI. The recall cites a fire hazard from the heating element when the sugar receptacle is missing. Consumers should stop using the unit and pursue a refund.

Youbeien Crib Mobiles Recalled Due to Battery Ingestion Risk — Check Model RT668-17

YooxArmor Recalled 2,000+ Kids’ Helmets Sold on Amazon Over Head-Injury Risk (2025)

Five Below Recalls Tabletop Fire Pits for Risk of Serious Burn Injury

EnHomee Fabric 13-Drawer Dressers Recalled for Tip-Over and Entrapment Risk (2025)

This recall involves EnHomee Fabric 13-Drawer Dressers. The Fabric 13-Drawer Dressers are 55.12" W x 35.45" H x 11.02" D and come in rustic brown, white, black, and pink.

B Braun Medical ESPOCAN Spinal/Epidural Tray Recalled Over Lid Position Risk

Potential for the lid of the catheter connector to be in the incorrect position.

B Braun Medical Recall Expands for Perifix FX Epidural Tray and Catheter Over Lid Position Defect (Z

Potential for the lid of the catheter connector to be in the incorrect position.

B Braun Medical Recall: 60-Unit Anesthesia Tray Recalled for Catheter Connector Lid Position Issue

Potential for the lid of the catheter connector to be in the incorrect position.

B Braun Medical PERIFIX FX Epidural Tray Recalled for Lid-Position Issue (21,270 Units)

Potential for the lid of the catheter connector to be in the incorrect position.

B Braun Medical Recalls 2,840 Anesthesia Tray Kits Over Catheter Lid Defect (2025)

Potential for the lid of the catheter connector to be in the incorrect position.

B Braun Medical Recalls 0 CE17TKFSDT Epidural Tray Kit for Lid Position Hazard (2025)

Potential for the lid of the catheter connector to be in the incorrect position.

B Braun Medical PERIFIX FX Epidural Set Recalled for Lid-Position Defect in 2025

Potential for the lid of the catheter connector to be in the incorrect position.

Cardinal Health 200 Salem Sump Stomach Tubes Recalled Worldwide in 2025 for ARV Breakage

Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.

Cardinal Health 200 Recalls Salem Sump Dual-Lumen Stomach Tubes Over ARV Breakage (2025)

Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.

Cardinal Health Salem Sump Stomach Tubes Recalled for ARV Breakage Risk (2025)

Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.

Cardinal Health Salem Sump PVC Tubes Recalled for ARV Breakage Risk (2025)

Cardinal Health 200, LLC recalled Salem Sump PVC Tubes worldwide after ARV breakage complaints. The anti-reflux valve can break under excessive force during use. Clinicians and patients should stop using the device and await recall instructions.

Cook Medical Zenith Alpha 2 Thoracic Graft Recall Affects 695 Devices in 2025

Affected devices may contain PTFE coating scrapings. Scrapings could be released during device deployment, potentially causing intravascular embolization.

B Braun Medical Perifix FX Epidural Tray Recall for Lid Misalignment in Catheter Connector

Potential for the lid of the catheter connector to be in the incorrect position.

Cardinal Health 200 Salem Sump Anti-Reflux Valve Recalled for Breakage Risk (2025)

Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.