immediate action Recalls

Black Sheep Egg Company Recalls 23,400 Dozen Free Range Eggs Over Salmonella Risk (2025)

Black Sheep Egg Company Recall: 288,900 Dozen Free Range Grade AA Eggs Over Salmonella Risk

Arizer Solo II Portable Vaporizers Recalled for Fire and Burn Hazards (Canada-Imported)

Arizer recalled the Solo II portable vaporizer on 2025-09-18 after reports of overheating lithium-ion batteries. The recall targets units imported by 7111495 Canada. Consumers should stop using the device and pursue a free replacement.

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.

LXDHSTRA Recall Expands on 2025 LXDHSTRA Baby Loungers and Crib Bumpers Sold on Amazon

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

IcyBreeze Recall Expands Over Fire Hazard Risk in Portable Misting Fans (2025)

Taproom Gourmet 15lb Bulk Madison Mix Recalled Over Undeclared Allergens

No ingredient label. Product contains undeclared allergens (peanuts, almonds, wheat, and soy)

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.

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.

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.

GE Medical Systems LOGIQ P9 R4.5 Ultrasound System Recalled for Inaccurate Liver Readings (37 Units)

The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.

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 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.

GE Medical Systems LOGIQ P10 Ultrasound System Recalled for UGAP Data Inaccuracy (31 Units, 2025)

The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.

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.

Kirkland Signature Ahi Tuna Wasabi Poke Recalled Over Listeria Risk

Listeria monocytogenes. Recall was initiated after being notified by green onion supplier of a Listeria monocytogenes positive test result in the green onions which were used only in Ahi Tuna Wasabi Poke.

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.